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[ CAS No. 4319-87-3 ] {[proInfo.proName]}

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Chemical Structure| 4319-87-3
Chemical Structure| 4319-87-3
Structure of 4319-87-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4319-87-3 ]

CAS No. :4319-87-3 MDL No. :MFCD19382397
Formula : C6H7BrN2O Boiling Point : -
Linear Structure Formula :- InChI Key :YDPPNMNAHGZFDJ-UHFFFAOYSA-N
M.W : 203.04 Pubchem ID :56592978
Synonyms :

Calculated chemistry of [ 4319-87-3 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.19
TPSA : 35.01 Ų

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) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.19
Log Po/w (XLOGP3) : 1.6
Log Po/w (WLOGP) : 1.56
Log Po/w (MLOGP) : 0.85
Log Po/w (SILICOS-IT) : 1.99
Consensus Log Po/w : 1.64

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.48
Solubility : 0.665 mg/ml ; 0.00327 mol/l
Class : Soluble
Log S (Ali) : -1.95
Solubility : 2.3 mg/ml ; 0.0113 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.02
Solubility : 0.192 mg/ml ; 0.000944 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.75

Safety of [ 4319-87-3 ]

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

Application In Synthesis of [ 4319-87-3 ]

* 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 [ 4319-87-3 ]
  • Downstream synthetic route of [ 4319-87-3 ]

[ 4319-87-3 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 124-41-4 ]
  • [ 3438-55-9 ]
  • [ 4319-87-3 ]
YieldReaction ConditionsOperation in experiment
79% at 20℃; for 1 h; Sodium methoxide (25 wtpercent solution in methanol, 1.83 mL, 16.0 mmol) was added to a solution of 5-bromo-4-chloro-6-methylpyrimidine (1.85 g, 8.92 mmol) in methanol (50 mL) and the reaction was stirred at ambient temperature for 1 hour. The reaction was quenched by the addition of pH 7 buffer. The majority of the methanol was removed under reduced pressure. The aqueous portion was diluted with water and was extracted with diethyl ether three times. The combined organic extracts were washed with brine, dried over Na2S04, filtered and concentrated to afford 5- bromo-4-methoxy-6-methylpyrimidine (1.43 g, 79percent). 1H NMR (CDC13, 400 MHz): 8 8.48 (s, 1H); 4.00 (s, 3H); 2.54 (s, 3H). MS (ES) 204(M+1).
Reference: [1] Patent: WO2005/105814, 2005, A1, . Location in patent: Page/Page column 67-68
  • 2
  • [ 67-56-1 ]
  • [ 3438-55-9 ]
  • [ 4319-87-3 ]
Reference: [1] Synthesis, 2011, # 10, p. 1529 - 1531
  • 3
  • [ 3524-87-6 ]
  • [ 4319-87-3 ]
Reference: [1] Synthesis, 2011, # 10, p. 1529 - 1531
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