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[ CAS No. 38185-55-6 ] {[proInfo.proName]}

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Chemical Structure| 38185-55-6
Chemical Structure| 38185-55-6
Structure of 38185-55-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38185-55-6 ]

CAS No. :38185-55-6 MDL No. :MFCD11110443
Formula : C5H4BrClN2 Boiling Point : -
Linear Structure Formula :- InChI Key :VXCUGLKQXLPHKI-UHFFFAOYSA-N
M.W : 207.46 Pubchem ID :12370669
Synonyms :

Calculated chemistry of [ 38185-55-6 ]      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) : -6.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 1.82
Log Po/w (WLOGP) : 2.09
Log Po/w (MLOGP) : 1.6
Log Po/w (SILICOS-IT) : 2.03
Consensus Log Po/w : 1.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.77
Solubility : 0.355 mg/ml ; 0.00171 mol/l
Class : Soluble
Log S (Ali) : -2.26
Solubility : 1.15 mg/ml ; 0.00553 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 : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.71

Safety of [ 38185-55-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 38185-55-6 ]

* 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 [ 38185-55-6 ]

[ 38185-55-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 12775-96-1 ]
  • [ 38185-55-6 ]
  • [ 39903-01-0 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; In tetrahydrofuran; diethylene glycol dimethyl ether; cyclohexane; ethylene glycol; ethyl acetate; EXAMPLE 5 A mixture of 5 parts of 2-amino-3-chloro-5-bromopyridine, 20 parts of potassium hydroxide (85percent), 3 parts of diethylene glycol dimethyl ether, 0.3 part of copper-bronze and 40 parts of glycol is stirred under nitrogen for 7 hours at 170°-175° C. After cooling, the dark-coloured solution is neutralised with concentrated hydrochloric acid, saturated with sodium chloride and extracted twice in the warm state with ethyl acetate/tetrahydrofuran (9:1). The organic layer is extracted by shaking with a saturated sodium chloride solution; the ethyl acetate phase is then filtered through Hyflo, dried with magnesium sulphate and purified with active charcoal. The clear yellow solution is concentrated almost to dryness and chromatographed through a short silica-gel column with ethyl acetate/cyclohexane (2:1). The yield is 2 parts of 2-amino-3-hydroxy-5-bromopyridine, m.p. 204°-207° C. (44.1percent of theory).
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