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[ CAS No. 13327-56-5 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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3d Animation Molecule Structure of 13327-56-5
Chemical Structure| 13327-56-5
Chemical Structure| 13327-56-5
Structure of 13327-56-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13327-56-5 ]

CAS No. :13327-56-5 MDL No. :MFCD00039900
Formula : C6H12O2S Boiling Point : -
Linear Structure Formula :- InChI Key :YSNWHRKJEKWJNY-UHFFFAOYSA-N
M.W : 148.22 Pubchem ID :61592
Synonyms :

Calculated chemistry of [ 13327-56-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.83
TPSA : 51.6 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.44 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.18
Log Po/w (XLOGP3) : 1.07
Log Po/w (WLOGP) : 1.3
Log Po/w (MLOGP) : 1.27
Log Po/w (SILICOS-IT) : 1.28
Consensus Log Po/w : 1.42

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.1
Solubility : 11.7 mg/ml ; 0.0789 mol/l
Class : Very soluble
Log S (Ali) : -1.75
Solubility : 2.67 mg/ml ; 0.018 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.65
Solubility : 3.33 mg/ml ; 0.0225 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.96

Safety of [ 13327-56-5 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P280-P370+P378-P403+P235-P501 UN#:1993
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13327-56-5 ]

* 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 [ 13327-56-5 ]

[ 13327-56-5 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 74-93-1 ]
  • [ 6414-69-3 ]
  • [ 13327-56-5 ]
  • 3
  • [ 13327-56-5 ]
  • [ 646-01-5 ]
  • 4
  • [ 74-93-1 ]
  • [ 140-88-5 ]
  • [ 13327-56-5 ]
  • 5
  • [ 1609-40-1 ]
  • [ 121-45-9 ]
  • [ 13327-56-5 ]
  • 6
  • [ 59-48-3 ]
  • [ 13327-56-5 ]
  • 3-[1-Hydroxy-3-methylsulfanyl-prop-(Z)-ylidene]-1,3-dihydro-indol-2-one [ No CAS ]
  • 7
  • [ 2373-51-5 ]
  • [ 65946-52-3 ]
  • [ 75-77-4 ]
  • [ 13327-56-5 ]
  • 8
  • [ 13327-56-5 ]
  • [ 28944-85-6 ]
  • (2E,5E)-3,5-Dimethyl-4-(2-methylsulfanyl-ethyl)-hepta-2,5-dien-4-ol [ No CAS ]
  • 9
  • [ 7647-01-0 ]
  • [ 13327-56-5 ]
  • [ 111-17-1 ]
  • [ 75-18-3 ]
  • 11
  • [ 13327-56-5 ]
  • [ 52754-04-8 ]
YieldReaction ConditionsOperation in experiment
98% With (4S,4aS,8aS)-5-ethyl-3-methyl-2?,4?:3?,5?-di-O-methylenedioxyriboflavinium perchlorate; dihydrogen peroxide; In methanol; water; at 20℃; for 8.0h; General procedure: A 30% aqueous solution of hydrogen peroxide (1.5 mL, 1.5 equiv) was added dropwise to a stirred mixture of sulfide (1.0 mmol) and 1 (11 mg, 0.02 mmol) in MeOH (1mL), and the mixture was stirred at ambient temperature. The progress of the reaction was monitored using gas-liquid chromatography (GLC) periodically. After the sulfide was found to be consumed, the reaction was quenched by the addition of a saturated Na2SO3 aqueous solution (1 mL) to decompose the remaining hydrogen peroxide. The reaction mixture was extracted with CH2Cl2 (1 mL × 2), dried over MgSO4, and evaporated under reduced pressure to afford sulfoxide. Structures and purity of sulfoxides were confirmed by comparison of their physical and spectral data with those reported in the literatures.
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