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[ CAS No. 36635-66-2 ] {[proInfo.proName]}

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Excepted Quantity USD 0.00
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Chemical Structure| 36635-66-2
Chemical Structure| 36635-66-2
Structure of 36635-66-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 36635-66-2 ]

CAS No. :36635-66-2 MDL No. :MFCD04114776
Formula : C15H13NO2S Boiling Point : -
Linear Structure Formula :- InChI Key :KIJCBVOPJSHLBI-UHFFFAOYSA-N
M.W : 271.33 Pubchem ID :10967613
Synonyms :

Calculated chemistry of [ 36635-66-2 ]

Physicochemical Properties

Num. heavy atoms : 19
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.13
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 73.31
TPSA : 42.52 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.82 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 3.01
Log Po/w (WLOGP) : 4.14
Log Po/w (MLOGP) : 2.9
Log Po/w (SILICOS-IT) : 1.94
Consensus Log Po/w : 2.4

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.69
Solubility : 0.0557 mg/ml ; 0.000205 mol/l
Class : Soluble
Log S (Ali) : -3.57
Solubility : 0.0734 mg/ml ; 0.000271 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.36
Solubility : 0.00117 mg/ml ; 0.00000433 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 3.38

Safety of [ 36635-66-2 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501 UN#:2811
Hazard Statements:H301-H311-H331 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 36635-66-2 ]

* 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.

  • Upstream synthesis route of [ 36635-66-2 ]
  • Downstream synthetic route of [ 36635-66-2 ]

[ 36635-66-2 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 37643-54-2 ]
  • [ 36635-66-2 ]
YieldReaction ConditionsOperation in experiment
48%
Stage #1: With trichlorophosphate In tetrahydrofuran at 25℃; for 0.0833333 h;
Stage #2: With triethylamine In tetrahydrofuran at 0 - 10℃; for 0.75 h;
A 500 ml, three-necked, flask fitted with athermometer was charged with N-(a-tosylbenzyl)formamide (16.73 g, 57.8 mmol) and dryTHF (120 ml). Phosphorus oxychloride (10.78 ml, 116.0 mmol) was added via syringeand resulting solution allowed to stir for 5 min at 25 °C. After cooling the solution to ca. 0oc with an ice/salt bath, triethylamine (48.4 ml, 347.0 mmol) was added by means of adropping funnel over 45 min whilst keeping the internal temperature below 10 °C. Afterthe triethylamine addition was complete, the reaction was stirred for 45 min at 5-10 oc(ice bath). Ethyl acetate (85 ml) then water (85 ml) was added to the reaction, themixture stirred for 5 min and, after transferring the mixture to a separatory funnel, theaqueous layer removed. The organic phase was washed with water (2x85 ml),saturated sodium bicarbonate solution (85 ml), brine (50 ml) and concentrated underreduced pressure until a slurry remained. The residue was diluted with n-propanol (85ml) and concentrated to half its original volume. The precipitate was cooled to 0 oc for15 min, collected on a Buchner funnel, washed with n-propanol (2x50 ml) and dried invacuo. This afforded a-tosylbenzylisocyanide (7.47 g, 48percent) as a beige solid. 1H NMR(200 MHz, CDCb) o 7.60 (d, 2H, J=8.2 Hz) 7.30-7.52 (m, ?H), 5.61 (s, 1 H), 2.47 (s, 3H).
Reference: [1] Patent: WO2018/53588, 2018, A1, . Location in patent: Paragraph 00101
[2] Tetrahedron Letters, 1996, vol. 37, # 45, p. 8113 - 8116
[3] Patent: WO2005/80380, 2005, A1, . Location in patent: Page/Page column 28-29
[4] Patent: WO2004/14900, 2004, A1, . Location in patent: Page 27
[5] Organic Syntheses, 2000, vol. 77, p. 198 - 198
  • 2
  • [ 536-57-2 ]
  • [ 36635-66-2 ]
Reference: [1] Tetrahedron Letters, 1996, vol. 37, # 45, p. 8113 - 8116
[2] Organic Syntheses, 2000, vol. 77, p. 198 - 198
[3] Patent: WO2018/53588, 2018, A1,
  • 3
  • [ 824-79-3 ]
  • [ 36635-66-2 ]
Reference: [1] Organic Syntheses, 2000, vol. 77, p. 198 - 198
[2] Patent: WO2018/53588, 2018, A1,
  • 4
  • [ 88333-03-3 ]
  • [ 455-16-3 ]
  • [ 36635-66-2 ]
Reference: [1] Journal of Organic Chemistry, 1977, vol. 42, # 7, p. 1153 - 1159
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