Home Cart 0 Sign in  

[ CAS No. 534-73-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 534-73-6
Chemical Structure| 534-73-6
Structure of 534-73-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 534-73-6 ]

Related Doc. of [ 534-73-6 ]

Alternatived Products of [ 534-73-6 ]

Product Details of [ 534-73-6 ]

CAS No. :534-73-6 MDL No. :MFCD00083636
Formula : C12H24O11 Boiling Point : -
Linear Structure Formula :- InChI Key :SERLAGPUMNYUCK-YJOKQAJESA-N
M.W : 344.31 Pubchem ID :94169
Synonyms :

Calculated chemistry of [ 534-73-6 ]

Physicochemical Properties

Num. heavy atoms : 23
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 8
Num. H-bond acceptors : 11.0
Num. H-bond donors : 9.0
Molar Refractivity : 70.31
TPSA : 200.53 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -12.52 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.98
Log Po/w (XLOGP3) : -5.8
Log Po/w (WLOGP) : -5.76
Log Po/w (MLOGP) : -4.77
Log Po/w (SILICOS-IT) : -3.59
Consensus Log Po/w : -3.79

Druglikeness

Lipinski : 2.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 4.0
Bioavailability Score : 0.17

Water Solubility

Log S (ESOL) : 2.21
Solubility : 55500.0 mg/ml ; 161.0 mol/l
Class : Highly soluble
Log S (Ali) : 2.26
Solubility : 62100.0 mg/ml ; 180.0 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 4.2
Solubility : 5510000.0 mg/ml ; 16000.0 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 5.37

Safety of [ 534-73-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 534-73-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 534-73-6 ]

[ 534-73-6 ] Synthesis Path-Downstream   1~18

  • 1
  • [ 108-24-7 ]
  • [ 534-73-6 ]
  • [ 41897-25-0 ]
YieldReaction ConditionsOperation in experiment
With sodium acetate
  • 3
  • [ 534-73-6 ]
  • 2-O-α-D-glucopyranosyl-glycolaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
82% With lead(IV) acetate; acetic acid In dimethyl sulfoxide at -30℃; for 1h;
With lead(IV) acetate In water; acetic acid; acetone at -73℃; for 1h;
YieldReaction ConditionsOperation in experiment
Ionophorese in wss.Na-molybdatlsg.;
YieldReaction ConditionsOperation in experiment
at 80℃; Hydrolysis;
  • 6
  • [ 534-73-6 ]
  • [ 50-70-4 ]
  • [ 50-99-7 ]
YieldReaction ConditionsOperation in experiment
With isomaltase; pig intestinal sucrase In various solvent(s) at 37℃; for 24h;
  • 7
  • [ 50-70-4 ]
  • [ 57-50-1 ]
  • [ 20942-96-5 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With dextransucrase (EC 2.4.1.5) at 25℃;
  • 8
  • [ 534-73-6 ]
  • [ 2280-44-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: Pb(OAc)4 / H2O; acetic acid; acetone / 1 h / -73 °C 2: NH2NH2 / 24 h / 50 - 70 °C 3: saturated NaHCO3 4: 50mH H2SO4 / 1 h / 35 °C
  • 9
  • [ 534-73-6 ]
  • Acetic acid [(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxy-hex-(Z)-ylidene]-hydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: Pb(OAc)4 / H2O; acetic acid; acetone / 1 h / -73 °C 2: NH2NH2 / 24 h / 50 - 70 °C 3: saturated NaHCO3
  • 10
  • [ 534-73-6 ]
  • [ 815-96-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: Pb(OAc)4 / H2O; acetic acid; acetone / 1 h / -73 °C 2: NH2NH2 / 24 h / 50 - 70 °C
YieldReaction ConditionsOperation in experiment
100% 1.G Reduction of Oligosaccharides G. 6-O-α-D-glucopyranosyl-D-glucose (α-D-Glcp-(1-6)-D-Glc) This oligosaccharide (51.6 μmol) was dissolved in 1.0 mL distilled water. Sodium borohydride (1.0 mmol) was added and the solution left for 18 hours at room temperature (~22° C.). Distilled water (4.0 mL) was added, followed by 1.0 mL of 2.0M acetic acid. After 1 hour, the sample was loaded on a well-washed column (5.0 mL) of Dowex AG50W-X8, H+ form, 100-200 mesh, and the eluent collected. It was washed with three additional 5.0 mL washes of water. The total eluent was rotary evaporated to dryness. Boric acid was removed by rotary evaporation to dryness five times with approximately 10 mL of a solution containing 1.0% (vol/vol) acetic acid in methanol, followed by rotary evaporation to dryness three times with about 10 mL of methanol alone. The product was 6-O-α-D-glucopyranosyl-D-glucitol; 100.0% yield.
  • 12
  • [ 7440-02-0 ]
  • [ 7440-18-8 ]
  • [ 13718-94-0 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen In water 5 EXAMPLE 5 EXAMPLE 5 The following reagents were introduced into a stirred autoclave: 443 g Water; 110 g Isomaltulose, and 1,39 g 5% Ruthenium on Carbon (on dry basis) and 0.55 g Nickel (54%) on Carbon as catalysts. The autoclave was closed, purged with nitrogen and then hydrogen was introduced up to 10 atmosphere. The temperature was raised up to 120° C. The reaction ceased after 150 minutes, a complete conversion to Isomaltitol being obtained, consisting of 50.5% GPM and 49.5% GPS.
  • 13
  • [ 7440-18-8 ]
  • [ 13718-94-0 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen In water 3 EXAMPLE 3 EXAMPLE 3 The following reagents were introduced into a stirred autoclave: 227.6 g Water; 91.4 g Isomaltulose, and 0.86 g 5% Ruthenium on Carbon (on dry basis) and 1.83 g 54% Nickel on Carbon as catalysts. The autoclave was closed, purged with nitrogen and then hydrogen was introduced up to 16 atmospheres. The temperature was raised up to 120° C. The reaction ceased after 120 minutes, a complete conversion to Isomaltitol being obtained, consisting of 56.1% GPM and 43.9% GPS.
  • 14
  • [ 13718-94-0 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen In water 1 EXAMPLE 1 EXAMPLE 1 The following reagents were introduced into a stirred autoclave: 325 g Water; 125.6 g Isomaltulose, and 1.58 g Ruthenium on Carbon (on dry basis), as catalyst. The autoclave was closed, purged with nitrogen and then gaseous hydrogen was introduced up to 16 atmospheres, The temperature was raised up to 120° C. The reaction ceased after 60 minutes, a complete conversion to Isomaltitol being obtained, consisting of 42.9% of GPM and 57.1% of GPS.
With hydrogen In water 2 EXAMPLE 2 EXAMPLE 2 The following reagents were introduced into a stirred autoclave: 325 g Water; 125.6 g Isomaltulose, and 1.9 g 5% Ruthenium on Carbon (on dry basis), as catalyst. The autoclave was closed, purged with nitrogen and then hydrogen was introduced up to 16 atmospheres. The temperature was raised up to 120° C. The reaction ceased after 90 minutes, a complete conversion to Isomaltitol being obtained, consisting of 47.8% GPM and 52.2% GPS.
With hydrogen In water 4 EXAMPLE 4 EXAMPLE 4 The following reagents were introduced into a stirred autoclave: 275 g Water; 225 g Isomaltulose, and 1.25 g 5% Ruthenium on Carbon (on dry basis) as catalyst. The autoclave was closed, purged with nitrogen and then hydrogen was introduced up to 16 atmospheres. The temperature was raised up to 120° C. The reaction ceased after 45 minutes, a complete conversion to Isomaltitol being obtained, consisting of 46.3% GPM and 53.7% GPS.
With hydrogen In water 6 EXAMPLE 6 EXAMPLE 6 The following reagents were introduced into a stirred autoclave: 700 g Water; 300 g Isomaltulose, and 1 g 5% Ruthenium on Carbon (on dry basis) as catalyst. The autoclave was closed, purged with nitrogen and then hydrogen was introduced up to 14 atmospheres. The temperature was raised up to 100° C. The reaction ceased after 90 minutes, a complete conversion to Isomaltitol being obtained, consisting of 44.1% GPM and 55.9% GPS.

YieldReaction ConditionsOperation in experiment
85% The high isomaltose content syrup thus obtained was hydrogenated in accordance with the method in Experiment 36, followed by removing the Raney Nickel catalyst from the mixture. The resulting mixture was decolored with an activated charcoal, desalted for purification with ion-exchange resins in H- and OH-forms, concentrated, and dried in vacuo to obtain a high isomaltitol content powder in a yield of about 85%.
  • 16
  • [ 57-48-7 ]
  • [ 2280-44-6 ]
  • [ 57-50-1 ]
  • [ 499-40-1 ]
  • [ 51411-23-5 ]
  • [ 13718-94-0 ]
  • [ 20942-96-5 ]
  • [ 20942-99-8 ]
  • [ 69-65-8 ]
  • [ 50-70-4 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;nickel; In water; at 20 - 130℃; under 22502.3 Torr;Autoclave;Product distribution / selectivity; Hydrogenation of isomaltulose/trehalulose solution, 30% dry matter, 30 barTable 5746 g aqueous isomaltulose/trehalulose solution (30% dry matter) of the composition shown in Table 5 (quantification according to the method explained for Examples 1-4) was introduced into the autoclave reactor. At a temperature of 300C the solution was supplemented with 2.2 g, 9.0 g and 15.7 g of nickel catalyst (Degussa, BK 111 W), respectively, corresponding to 1%, 4% and 7% of catalyst, respectively, based on the dry sugar content of the isomaltulose/trehalulose solution. The reactor was closed and inertized 3 times with nitrogen. The nitrogen was exchanged with hydrogen 3 times and subsequently, the hydrogen pressure was adjusted to 30 bar. The rotation speed was increased to 1,220 rpm and the isomaltulose/trehalose mixture was heated from 300C to 1300C with a heating rate of 3C/min. Consumed hydrogen was automatically replenished so that the pressure of 30 bar was maintained throughout the course of the hydrogenation reaction. Samples were taken when the temperature of 1300C was reached having the compositions set out in Table 6 (quantification according to the method explained for Examples 1-3).Table 6 <n="16"/>It is evident from Table 6 that the GPM/GPS ratio is dependant on the catalyst concentration at constant heating rate. The ratio cis/trans isomer (GPM/GPS) decreases with increased catalyst concentration.The reaction containing 1% catalyst was continued for an additional hour at 13O0C in order to demonstrate that the reaction can be completed and the remaining isomaltulose content can be reduced below 0.05% without changing the obtained GPM/GPS ratio significantly.; Example 11Hydrogenation of isomaltulose/trehalulose solution, 30% dry matter, 30 bar746 g aqueous isomaltulose/trehalulose solution (30% dry matter) of a composition shown in Table 6 (, see Example 5; quantification according to the method explained for Examples 1-4), introduced into the autoclave reactor described above, was supplemented with 9.0 g nickel catalyst (Degussa, BK 111 W), corresponding to 4% of catalyst based on the dry matter content of the isomaltulose/trehalulose solution. The reactor was closed and inertized twice with nitrogen. The nitrogen was exchanged with hydrogen twice and subsequently, the hydrogen pressure was adjusted to 30 bar while mixing at 333 rpm. The rotation speed was increased to 1,220 rpm and the isomaltulose/ trehalulose solution was heated from about 2O0C to 1300C with various heating rates, respectively. Consumed hydrogen was automatically replenished so that the pressure of 30 bar was maintained during the course of the hydrogenation reaction. Samples were taken when the temperature of 1300C was reached, having the compositions set out in Table 14 (quantification according to the method explained for Examples 1-3). <n="23"/>Table 14It is evident from Table 14 that the GPM/GPS ratio is dependant on the heating rate of the reaction mixture.
  • 17
  • [ 57-48-7 ]
  • [ 2280-44-6 ]
  • [ 499-40-1 ]
  • [ 51411-23-5 ]
  • [ 13718-94-0 ]
  • [ 20942-96-5 ]
  • [ 20942-99-8 ]
  • [ 69-65-8 ]
  • [ 50-70-4 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;nickel; In water; at 20 - 130℃; under 22502.3 - 97509.8 Torr;Autoclave;Product distribution / selectivity; Hydrogenation of isomaltulose solution, 50% dry matter, 30 bar816 g aqueous isomaltulose solution (50% dry matter) was introduced into the autoclave reactor. At a temperature of 300C, the solution was supplemented with 4.1 g, 16.3 g and 28.6 g of nickel catalyst (Degussa, BK 111 W), respectively, corresponding to 1%, 4% and 7% of catalyst, respectively, based on the dry sugar content of the isomaltulose solution. The reactor was closed and inertized 3 times with nitrogen. The nitrogen was exchanged with hydrogen 3 times and subsequently, the hydrogen pressure was adjusted to 30 bar. The rotation speed was increased to 1,220 rpm and the isomaltulose solution was heated from 300C to 1300C with a heating rate of 3C/min. Consumed hydrogen was automatically replenished so that the pressure of 30 bar was maintained throughout the course of the hydrogenation reaction. Samples were taken when the temperature of 1300C was reached, having the compositions set out in Table 2.Table 2GPS*: GPS consists primarily of 1,6-GPS and minor amounts of 1,1-GPS, the latter being formed from trehalulose. 1,1-GPS and 1,6-GPS co-elute in the HPLC method used.It is evident from Table 2 that the GPM/GPS ratio is dependant on the catalyst concentration at constant heating rate. The ratio cis/trans isomer (GPM/GPS) decreases with increased catalyst concentrationThe reaction containing 1% catalyst was continued for an additional hour at 1300C in order to demonstrate that the reaction can be completed and the remaining <n="13"/>isomaltulose content can be reduced below 0.05% without changing the obtained GPM/GPS ratio significantly.; Example 2 Hydrogenation of isomaltulose solution, 50% dry matter, 130 bar816 g aqueous isomaltulose solution (50% dry matter) was introduced into the autoclave reactor. At a temperature of 300C the solution was supplemented with 4.1 g, 16.3 g and 28.6 g of nickel catalyst (Degussa, BK 111 W), respectively, corresponding to 1%, 4% and 7% of catalyst, respectively, based on the dry sugar content of the isomaltulose solution. The reactor was closed and inertized 3 times with nitrogen. The nitrogen was exchanged with hydrogen 3 times and subsequently, the hydrogen pressure was adjusted to 130 bar. The rotation speed was increased to 1,220 rpm and the isomaltulose solution was heated from 300C to 13O0C with a heating rate of 3C/min. Consumed hydrogen was automatically replenished so that the pressure of 130 bar was maintained throughout the course of the hydrogenation reaction. Samples were taken when the temperature of 1300C was reached, having the compositions set out in Table 3.Table 3It is evident from Table 3 that the GPM/GPS ratio is dependant on the catalyst concentration at constant heating rate. The ratio cis/trans isomer (GPM/GPS) decreases with increased catalyst concentration.; Example 3Hydrogenation of isomaltulose solution, 30% dry matter, 80 bar746 g aqueous isomaltulose solution (30% dry matter) was introduced into the autoclave reactor. At a temperature of 3O0C the solution was supplemented with 2.2 g, 9.0 g and 15.7 g of nickel catalyst (Degussa, BK 111 W), respectively, corresponding to 1%, 4% and 7% of catalyst, respectively, based on the dry sugar content of the isomaltulose solution. The reactor was closed an inertized 3 times with nitrogen. The nitrogen was exchanged with hydrogen 3 times and subsequently, the hydrogen pressure was adjusted to 80 bar. The rotation speed was increased to 1,220 rpm and the isomaltulose solution was heated from 300C to 1300C with a heating rate of 3C/min. Consumed hydrogen was automatically replenished so that the pressure of 80 bar was maintained throughout the course of the hydrogenation reaction. The samples were taken when the temperature of 1300C was reached, having the compositions set out in table 4.Table 4It is evident from table 4 that the GPM/GPS ratio is dependent on the catalyst concentration at constant heating rate. The ratio cis/trans isomer (GPM/GPS) decreases with increased catalyst concentration.; Examples 6-8The following embodiments of the present invention relate to a process for the preparation of a mixture of the stereoisomeric sugar alcohols 6-O-alpha-D- glucopyranosyl-D-sorbitol (1,6-GPS) and 1-O-alpha-D-glucopyranosyl-D-mannitol (1,1- GPM) by hydrogenation of isomaltulose using a Raney nickel catalyst at increased hydrogen pressure, wherein the ratio of 1,6-GPS/1,1-GPM can be regulated by changing the heating rate of the reaction mixture. The isomaltulose reagent is specified in Table 1 (supra). The isomaltulose was hydrogenated as described for Examples 1-3 with different starting temperatures as mentioned in the following examples. For analysis of the obtained hydrogenation product samples, the same procedures were utilized as stated above. <n="18"/>Example 6Hydrogenation of isomaltulose solution, 30% dry matter, 30 bar746 g aqueous isomaltulose solution (30% dry matter), introduced into the autoclave reactor, was supplemented with 9...
  • 18
  • [ 13718-94-0 ]
  • [ 20942-99-8 ]
  • [ 534-73-6 ]
YieldReaction ConditionsOperation in experiment
81.818 % de With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; dichloro(benzene)ruthenium(II) dimer; hydrogen In methanol at 100℃; for 16h; Autoclave; Overall yield = 84 percent; Overall yield = 1.14 g; diastereoselective reaction;
50 % de With (S)-(+)-5,5’-bis[di(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-4,4’-bi-1,3-benzodioxole; dichloro(benzene)ruthenium(II) dimer; hydrogen In methanol at 100℃; for 16h; Autoclave; diastereoselective reaction;
Same Skeleton Products
Historical Records

Related Functional Groups of
[ 534-73-6 ]

Ethers

Chemical Structure| 63864-94-8

[ 63864-94-8 ]

(3R,4R,5R,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 24332-98-7

[ 24332-98-7 ]

(2S,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 116183-64-3

[ 116183-64-3 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6S)-6-(Dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 14687-15-1

[ 14687-15-1 ]

(2R,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 106402-05-5

[ 106402-05-5 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-4,5-Dihydroxy-2-(hydroxymethyl)-6-(nonyloxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Alcohols

Chemical Structure| 25320-93-8

[ 25320-93-8 ]

(2S,3R,4S,5S,6R)-2-Butoxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 24332-98-7

[ 24332-98-7 ]

(2S,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 116183-64-3

[ 116183-64-3 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6S)-6-(Dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 14687-15-1

[ 14687-15-1 ]

(2R,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 106402-05-5

[ 106402-05-5 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-4,5-Dihydroxy-2-(hydroxymethyl)-6-(nonyloxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Related Parent Nucleus of
[ 534-73-6 ]

Tetrahydropyrans

Chemical Structure| 25320-93-8

[ 25320-93-8 ]

(2S,3R,4S,5S,6R)-2-Butoxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 24332-98-7

[ 24332-98-7 ]

(2S,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 116183-64-3

[ 116183-64-3 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6S)-6-(Dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 14687-15-1

[ 14687-15-1 ]

(2R,3S,4R,5S,6S)-2-Methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00

Chemical Structure| 106402-05-5

[ 106402-05-5 ]

(2R,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6R)-4,5-Dihydroxy-2-(hydroxymethyl)-6-(nonyloxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Similarity: 1.00