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[ CAS No. 170235-26-4 ] {[proInfo.proName]}

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Chemical Structure| 170235-26-4
Chemical Structure| 170235-26-4
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Product Details of [ 170235-26-4 ]

CAS No. :170235-26-4 MDL No. :MFCD06659908
Formula : C5H4BrNO2S Boiling Point : -
Linear Structure Formula :- InChI Key :YOWKNNKTQWCYNC-UHFFFAOYSA-N
M.W : 222.06 Pubchem ID :2763213
Synonyms :

Calculated chemistry of [ 170235-26-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.2
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.09
TPSA : 67.43 ?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) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.95
Log Po/w (XLOGP3) : 2.16
Log Po/w (WLOGP) : 1.69
Log Po/w (MLOGP) : 0.47
Log Po/w (SILICOS-IT) : 2.62
Consensus Log Po/w : 1.78

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.82
Solubility : 0.34 mg/ml ; 0.00153 mol/l
Class : Soluble
Log S (Ali) : -3.21
Solubility : 0.137 mg/ml ; 0.000618 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.23
Solubility : 1.31 mg/ml ; 0.00589 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.79

Safety of [ 170235-26-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 170235-26-4 ]

* 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 [ 170235-26-4 ]
  • Downstream synthetic route of [ 170235-26-4 ]

[ 170235-26-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 170235-26-4 ]
  • [ 5198-86-7 ]
YieldReaction ConditionsOperation in experiment
49% at 0 - 90℃; for 1.33 h; Inert atmosphere A solution of methyl 2-bromothiazole-4-carboxylate (0.500 g, 2.25 mmol) in EtOH (10 mL) in a 50 mL flask under a nitrogen atmosphere was cooled to 0 °C and treated with NaBH4 (170 mg, 4.50 mmol) portion- wise over 5 min. After stirring for 15 min at 0 °C, the reaction mixture was heated at 90 °C for 1 h. The cooled mixture was then quenched with saturated aqueous NH4C1 (15 mL) and stirring was continued for 20 min. Ethyl acetate (50 mL) was then added and the organic phase was separated, washed with brine, dried over MgS04 and concentrated to give the title compound (0.212 g, 49percent) which was used as such in the next step. 1H NMR (CDCl3, 400 MHz) δ ppm: 7.18 (s, 1H), 4.76 (s, 2H), 2.21 (br s, 1H).
Reference: [1] Patent: WO2013/163279, 2013, A1, . Location in patent: Paragraph 00177
[2] Patent: WO2016/138199, 2016, A1, . Location in patent: Paragraph 0084
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