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[ CAS No. 5140-72-7 ] {[proInfo.proName]}

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Chemical Structure| 5140-72-7
Chemical Structure| 5140-72-7
Structure of 5140-72-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5140-72-7 ]

CAS No. :5140-72-7 MDL No. :MFCD00181262
Formula : C5H3BrClN Boiling Point : -
Linear Structure Formula :- InChI Key :JWTZSVLLPKTZJP-UHFFFAOYSA-N
M.W : 192.44 Pubchem ID :78820
Synonyms :

Calculated chemistry of [ 5140-72-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.95
TPSA : 12.89 ?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) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.97
Log Po/w (XLOGP3) : 2.21
Log Po/w (WLOGP) : 2.5
Log Po/w (MLOGP) : 1.85
Log Po/w (SILICOS-IT) : 2.76
Consensus Log Po/w : 2.26

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.98
Solubility : 0.201 mg/ml ; 0.00105 mol/l
Class : Soluble
Log S (Ali) : -2.12
Solubility : 1.48 mg/ml ; 0.00767 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.5
Solubility : 0.0614 mg/ml ; 0.000319 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.93

Safety of [ 5140-72-7 ]

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

Application In Synthesis of [ 5140-72-7 ]

* 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 [ 5140-72-7 ]

[ 5140-72-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22929-52-8 ]
  • [ 5140-72-7 ]
  • 3-(6-chloropyridin-2-yl)tetrahydrofuran-3-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% 2-Bromo-6-chloropyridine (44.44 g, 231 mmol) was dissolved in dichloromethane (DCM) (770 mL),Stir in a three-necked 2L reaction flask,It was then cooled to -78 C.n-Butyllithium (1M in THF) (106 mL, 266 mmol) was cannulated into the addition funnel and then added dropwise into the reaction while maintaining the temperature below -69 C.The reaction was stirred for 20 minutes.Dihydrofuran-3 (2H) -one (22.86 g, 266 mmol) was dissolved in a minimum amount of DCM and then added dropwise into the reaction.The reaction was slowly warmed to room temperature.After the reaction reaches room temperature,This was quenched with ammonium chloride solution (200 mL) and then the layers were separated.The aqueous layer was extracted with DCM and then the organic layer was washed with brine (200 mL). The organic layer was dried over MgSO4 and then concentrated to dryness. The crude residue was purified by silica gel chromatography eluting with 0% to 100% ethyl acetate in heptane to give the product (33.5 g, 71% yield).
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