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[ CAS No. 1211516-25-4 ] {[proInfo.proName]}

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Chemical Structure| 1211516-25-4
Chemical Structure| 1211516-25-4
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Product Details of [ 1211516-25-4 ]

CAS No. :1211516-25-4 MDL No. :MFCD18257503
Formula : C7H6BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :WMNTYVZHTYHFLX-UHFFFAOYSA-N
M.W : 216.03 Pubchem ID :71721002
Synonyms :

Calculated chemistry of [ 1211516-25-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.86
TPSA : 50.19 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
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) : 1.36
Log Po/w (XLOGP3) : 2.1
Log Po/w (WLOGP) : 1.85
Log Po/w (MLOGP) : -0.02
Log Po/w (SILICOS-IT) : 1.85
Consensus Log Po/w : 1.43

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.84
Solubility : 0.312 mg/ml ; 0.00145 mol/l
Class : Soluble
Log S (Ali) : -2.78
Solubility : 0.355 mg/ml ; 0.00164 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.65
Solubility : 0.489 mg/ml ; 0.00226 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.88

Safety of [ 1211516-25-4 ]

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

Application In Synthesis of [ 1211516-25-4 ]

* 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 [ 1211516-25-4 ]

[ 1211516-25-4 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 450844-27-6 ]
  • [ 1211516-25-4 ]
YieldReaction ConditionsOperation in experiment
63.8%
Stage #1: at 120℃;
Stage #2: With hydrogenchloride In water
6-Bromo-5-methyl-pyridine-2-carbonitrile (1.0 g, 5.0 mmol) was added to a solution of sodium hydroxide (0.3 g, 7 mmol) in water (20 mL), the mixture was stirred at 120° C. overnight. Subsequently, the mixture was adjusted to pH=3 and extracted with ethyl acetate (2.x.15 mL). The organic extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated to give the product (0.7 g, 63.8percent); MS (EI): m/e 216.0 [M+H]+.
Reference: [1] Patent: US2012/316147, 2012, A1, . Location in patent: Page/Page column 52
[2] Patent: WO2012/168350, 2012, A1, . Location in patent: Page/Page column 114
  • 2
  • [ 1620-77-5 ]
  • [ 1211516-25-4 ]
Reference: [1] Patent: US2012/316147, 2012, A1,
[2] Patent: WO2012/168350, 2012, A1,
  • 3
  • [ 2369-19-9 ]
  • [ 1211516-25-4 ]
Reference: [1] Patent: US2012/316147, 2012, A1,
[2] Patent: WO2012/168350, 2012, A1,
  • 4
  • [ 159727-87-4 ]
  • [ 1211516-25-4 ]
Reference: [1] Patent: US2012/316147, 2012, A1,
[2] Patent: WO2012/168350, 2012, A1,
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