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[ CAS No. 14667-47-1 ] {[proInfo.proName]}

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Chemical Structure| 14667-47-1
Chemical Structure| 14667-47-1
Structure of 14667-47-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 14667-47-1 ]

CAS No. :14667-47-1 MDL No. :MFCD00128872
Formula : C7H8N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NZZDEODTCXHCRS-UHFFFAOYSA-N
M.W : 152.15 Pubchem ID :351633
Synonyms :

Calculated chemistry of [ 14667-47-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.92
TPSA : 65.21 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.49
Log Po/w (XLOGP3) : 1.86
Log Po/w (WLOGP) : 0.46
Log Po/w (MLOGP) : 0.15
Log Po/w (SILICOS-IT) : 0.47
Consensus Log Po/w : 0.89

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.23
Solubility : 0.903 mg/ml ; 0.00593 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.215 mg/ml ; 0.00141 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.73
Solubility : 2.87 mg/ml ; 0.0188 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 14667-47-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 14667-47-1 ]

* 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 [ 14667-47-1 ]
  • Downstream synthetic route of [ 14667-47-1 ]

[ 14667-47-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 14667-47-1 ]
  • [ 50735-34-7 ]
YieldReaction ConditionsOperation in experiment
99% With bromine; sodium hydrogencarbonate In dichloromethane at 0 - 20℃; for 1 h; To a stirred solution of 2-amino-nicotinic acid methyl ester (2 g, 13.15 mmol) and sodium bicarbonate (2.2 g, 26.31 mmol) in DCM (30 mL) is added a solution of bromine (1.01 mL in DCM (20 mL) drop wise at 0° C.
The reaction mixture is stirred at room temperature for 1 hour.
The reaction mixture is quenched with sodium bisulfite solution (50 mL) and extracted with DCM (2*40 mL).
The combined organic layers are washed with brine (40 mL), dried over sodium sulphate, filtered, and evaporated under reduced pressure to give the title compound as a yellow solid (3 g, 99percent). LCMS m/z (79Br/81Br) 231/233 (M+H)+.
Reference: [1] Patent: US2017/29420, 2017, A1, . Location in patent: Paragraph 0034
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