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[ CAS No. 105827-91-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 105827-91-6
Chemical Structure| 105827-91-6
Structure of 105827-91-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 105827-91-6 ]

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Product Details of [ 105827-91-6 ]

CAS No. :105827-91-6 MDL No. :MFCD01073549
Formula : C4H3Cl2NS Boiling Point : No data available
Linear Structure Formula :- InChI Key :VRMUIVKEHJSADG-UHFFFAOYSA-N
M.W : 168.04 Pubchem ID :2763179
Synonyms :

Calculated chemistry of [ 105827-91-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.89
TPSA : 41.13 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.94
Log Po/w (XLOGP3) : 2.34
Log Po/w (WLOGP) : 2.38
Log Po/w (MLOGP) : 1.11
Log Po/w (SILICOS-IT) : 3.77
Consensus Log Po/w : 2.31

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.75
Solubility : 0.297 mg/ml ; 0.00177 mol/l
Class : Soluble
Log S (Ali) : -2.84
Solubility : 0.241 mg/ml ; 0.00144 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.92
Solubility : 0.2 mg/ml ; 0.00119 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.66

Safety of [ 105827-91-6 ]

Signal Word:Danger Class:8,6.1
Precautionary Statements:P501-P273-P272-P260-P270-P202-P201-P264-P280-P391-P308+P313-P361+P364-P303+P361+P353-P333+P313-P301+P330+P331-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405 UN#:2922
Hazard Statements:H311-H302-H314-H317-H341-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 105827-91-6 ]

* 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 [ 105827-91-6 ]

[ 105827-91-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1196473-37-6 ]
  • [ 105827-91-6 ]
  • [ 1296850-08-2 ]
YieldReaction ConditionsOperation in experiment
35% H181 (0.667mmol) was dissolved in DMF (lOmL) and cooled to 0°C with ice bath. To this solution under nitrogen were added in sequence sodium hydride (106mg, 2.67mmol, 4.0eq) and 2-chloro-5-(chloromethyl)thiazole (0.298mL,2.67mmol, 4.0eq). The reaction mixture was stirred for 4 hours then treated with 1M HC1 (10ml). After extraction with ethyl acetate, the organic layer was washed with water and brine, and dried over anhydrous Na2S04. The residue after rotary evaporation was purified by column chromatography over silica gel to give the title compound (66mg, 35percent yield). 1H NMR (400 MHz, DMSO-d6): delta 9.16 (s, 1H), 7.92 (d, J = 4 Hz, 1H), 7.34 (d, J = 8.8 Hz, 2H), 7.13 (dd, J = 8.0 2.7 Hz, 1H), 5.35 (s, 2H) and 4.92 (s, 2H) ppm. Mp 112-114°C.
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