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[ CAS No. 56962-00-6 ] {[proInfo.proName]}

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Chemical Structure| 56962-00-6
Chemical Structure| 56962-00-6
Structure of 56962-00-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 56962-00-6 ]

CAS No. :56962-00-6 MDL No. :MFCD11848418
Formula : C6H6ClNO Boiling Point : -
Linear Structure Formula :- InChI Key :JSHJJLQJRLNBBA-UHFFFAOYSA-N
M.W : 143.57 Pubchem ID :19828962
Synonyms :

Calculated chemistry of [ 56962-00-6 ]      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 : 2.0
Molar Refractivity : 37.88
TPSA : 46.25 ?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 : Yes
Log Kp (skin permeation) : -5.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.29
Log Po/w (XLOGP3) : 1.84
Log Po/w (WLOGP) : 1.64
Log Po/w (MLOGP) : 1.41
Log Po/w (SILICOS-IT) : 1.31
Consensus Log Po/w : 1.5

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.38
Solubility : 0.595 mg/ml ; 0.00414 mol/l
Class : Soluble
Log S (Ali) : -2.43
Solubility : 0.531 mg/ml ; 0.0037 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.06
Solubility : 1.26 mg/ml ; 0.00881 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.1

Safety of [ 56962-00-6 ]

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 [ 56962-00-6 ]

* 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 [ 56962-00-6 ]

[ 56962-00-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 56962-00-6 ]
  • [ 858854-82-7 ]
  • 2
  • [ 56962-00-6 ]
  • [ 122-51-0 ]
  • [ 943443-12-7 ]
YieldReaction ConditionsOperation in experiment
88% at 105℃; for 4h; Triethyl orthoformate (3 mL) was added to the compound obtained in b) (574 mg, 4 mmol), and the resulting mixture was stirred at 105 C. for 4 hours. The reaction mixture was left to cool to room temperature, and the resulting residue was purified by silica gel column chromatography to obtain crystals of the title compound (538 mg, yield 88%). 1H-NMR (CDCl3) δ: 7.3-7.4 (2H, 7.52 (1H, dd, J=1.4 Hz, 7.8 Hz), 8,15 (1H, s)
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