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[ CAS No. 6388-47-2 ] {[proInfo.proName]}

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Chemical Structure| 6388-47-2
Chemical Structure| 6388-47-2
Structure of 6388-47-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6388-47-2 ]

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Product Details of [ 6388-47-2 ]

CAS No. :6388-47-2 MDL No. :MFCD00134229
Formula : C7H6ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :LWUAMROXVQLJKA-UHFFFAOYSA-N
M.W : 171.58 Pubchem ID :80807
Synonyms :

Calculated chemistry of [ 6388-47-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 42.82
TPSA : 63.32 ?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) : -5.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.3
Log Po/w (XLOGP3) : 1.95
Log Po/w (WLOGP) : 1.63
Log Po/w (MLOGP) : 0.48
Log Po/w (SILICOS-IT) : 1.14
Consensus Log Po/w : 1.3

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.47
Solubility : 0.581 mg/ml ; 0.00339 mol/l
Class : Soluble
Log S (Ali) : -2.9
Solubility : 0.214 mg/ml ; 0.00125 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.02
Solubility : 1.63 mg/ml ; 0.00948 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.1

Safety of [ 6388-47-2 ]

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 [ 6388-47-2 ]

* 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 [ 6388-47-2 ]

[ 6388-47-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 52023-68-4 ]
  • [ 6388-47-2 ]
  • 8-chloro-3-(6-morpholinopyridin-3-yl)quinazolin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
14% With trimethyl orthoformate; In tetrahydrofuran; at 110℃; for 18h;Sealed tube; General procedure: 3-Chloroanthranilic acid was taken in a sealed tube together with trimethyl orthoformate (1.2 equiv), aromatic amine (1.2 equiv), and THF, and the resulting reaction mixture was heated at 110C for 18h. It was cooled down to room temperature, saturated sodium bicarbonate solution was added, and the crude product was extracted with ethyl acetate. The combined organic layer was dried with magnesium sulfate, filtered, concentrated under reduced pressure, and purified through flash column chromatography.
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