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[ CAS No. 169833-70-9 ] {[proInfo.proName]}

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Chemical Structure| 169833-70-9
Chemical Structure| 169833-70-9
Structure of 169833-70-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 169833-70-9 ]

CAS No. :169833-70-9 MDL No. :MFCD04971930
Formula : C5H4BrClN2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YCECOMBEVDPUJG-UHFFFAOYSA-N
M.W : 207.46 Pubchem ID :2050085
Synonyms :

Calculated chemistry of [ 169833-70-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.35
TPSA : 38.91 ?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) : -6.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.61
Log Po/w (XLOGP3) : 2.16
Log Po/w (WLOGP) : 2.09
Log Po/w (MLOGP) : 1.19
Log Po/w (SILICOS-IT) : 2.03
Consensus Log Po/w : 1.82

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.98
Solubility : 0.217 mg/ml ; 0.00105 mol/l
Class : Soluble
Log S (Ali) : -2.61
Solubility : 0.51 mg/ml ; 0.00246 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.14
Solubility : 0.15 mg/ml ; 0.000724 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.09

Safety of [ 169833-70-9 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 169833-70-9 ]

* 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 [ 169833-70-9 ]

[ 169833-70-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13250-46-9 ]
  • [ 169833-70-9 ]
  • [ 1112982-76-9 ]
YieldReaction ConditionsOperation in experiment
In isopropyl alcohol; at 80℃; for 16h; As shown in step 4-i of Scheme 4, acetylisothiocyanate (6.824 g, 67.48 mmol) was added to a solution of 6-bromo-2-chloropyridin-3 -amine (14.0 g, 67.48 mmol) in isopropanol (300 mL). The reaction was heated for 16 hours at 80 0C. LCMS analysis indicated that the resulting mixture contained 85% desired product and 15% intermediate thiourea. The reaction mixture was cooled to RT, filtered, and the filtration cake washed with saturated sodium bicarbonate solution and brine. The solid was air dried to yield N-(5- <n="36"/>bromothiazolo[5,4-6]pyridin-2-yl)acetamide (Compound 1005, 12.0 g): 1H NMR (DMSOd6) delta 8.10(d, IH), 7.68(d, IH), 2.3(s, 3H).
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