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[ CAS No. 798545-30-9 ] {[proInfo.proName]}

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Chemical Structure| 798545-30-9
Chemical Structure| 798545-30-9
Structure of 798545-30-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 798545-30-9 ]

CAS No. :798545-30-9 MDL No. :MFCD08437553
Formula : C10H6BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :HVNYDSMSHWJYHG-UHFFFAOYSA-N
M.W : 252.06 Pubchem ID :17039590
Synonyms :

Calculated chemistry of [ 798545-30-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 56.4
TPSA : 50.19 ?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) : -6.13 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.7
Log Po/w (XLOGP3) : 2.4
Log Po/w (WLOGP) : 2.7
Log Po/w (MLOGP) : 0.93
Log Po/w (SILICOS-IT) : 2.47
Consensus Log Po/w : 2.04

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.38
Solubility : 0.106 mg/ml ; 0.000419 mol/l
Class : Soluble
Log S (Ali) : -3.1
Solubility : 0.202 mg/ml ; 0.000802 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.93
Solubility : 0.0295 mg/ml ; 0.000117 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.3

Safety of [ 798545-30-9 ]

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

Application In Synthesis of [ 798545-30-9 ]

* 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 [ 798545-30-9 ]

[ 798545-30-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 798545-30-9 ]
  • [ 1296950-96-3 ]
YieldReaction ConditionsOperation in experiment
92% Example 22 3-(4-Cyclobutyl-thiazol-2-yl)-quinoline-6-carboxylic acid Step 1 To a suspension of 6-bromoquinoline-3-carboxylic acid (0.50 g, 1.98 mmol) in dichloromethane (10 ml) was added oxalyl chloride (327 mg, 0.22 ml, 2.58 mmol) followed by DMF (3 drops). Gentle gas evolution was observed. The reaction mixture was stirred at room temperature for 2 h then concentrated to a white solid. The residue was suspended in diethyl ether (10 ml) and 28% ammonium hydroxide (2.0 ml, 16.0 mmol) was added. The mixture was stirred vigorously at room temperature for 2 h then filtered, rinsing with water and diethyl ether. Dried to by air then under high vacuum to afford 457 mg (92%) of 6-bromo-quinoline-3-carboxylic acid amide as a beige solid.
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