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[ CAS No. 61367-07-5 ] {[proInfo.proName]}

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Chemical Structure| 61367-07-5
Chemical Structure| 61367-07-5
Structure of 61367-07-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 61367-07-5 ]

CAS No. :61367-07-5 MDL No. :MFCD08274538
Formula : C8H16ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :NHAYDXCUCXRAMF-UHFFFAOYSA-N
M.W : 193.67 Pubchem ID :18521575
Synonyms :

Calculated chemistry of [ 61367-07-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 49.41
TPSA : 52.32 ?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) : -6.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.21
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 1.0
Log Po/w (SILICOS-IT) : 0.65
Consensus Log Po/w : 0.87

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.67
Solubility : 4.13 mg/ml ; 0.0213 mol/l
Class : Very soluble
Log S (Ali) : -1.91
Solubility : 2.41 mg/ml ; 0.0124 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.79
Solubility : 31.4 mg/ml ; 0.162 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.4

Safety of [ 61367-07-5 ]

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 [ 61367-07-5 ]

* 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 [ 61367-07-5 ]

[ 61367-07-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 97-08-5 ]
  • [ 61367-07-5 ]
  • [ 1310478-41-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 20℃; for 2h; Example 19(1r,4R)-4-(2-phenyl-1H-indole-6-sulfonamido)-N-((R)-1-(pyridin-2-yl)ethyl)cyclohexanecarboxamide Step 1. Preparation of (1r,4r)-methyl 4-(4-chloro-3-nitrophenylsulfonamido)cyclo hexanecarboxylate; (1r,4r)-methyl 4-aminocyclohexanecarboxylate HCl salt (7.75 g, 40 mmol) was suspended in a mixture of DCM (50 mL) and then treated with triethylamine (22.31 mL, 160 mmol), followed by 4-chloro-3-nitrobenzene-1-sulfonyl chloride (11.27 g, 44 mmol). The reaction mixture was stirred at rt for 2 h and then concentrated under reduced pressure. The residue was taken up in ethyl acetate (100 mL) and washed with 1N aq. HCl (3×100 mL), brine (100 mL) and dried over sodium sulfate. Filtration and concentration of the organic solution gave product (14.1 g) as a yellow solid (MS: (M+H)+=377.3).
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