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[ CAS No. 5292-21-7 ] {[proInfo.proName]}

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Chemical Structure| 5292-21-7
Chemical Structure| 5292-21-7
Structure of 5292-21-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5292-21-7 ]

CAS No. :5292-21-7 MDL No. :MFCD00001518
Formula : C8H14O2 Boiling Point : -
Linear Structure Formula :- InChI Key :LJOODBDWMQKMFB-UHFFFAOYSA-N
M.W : 142.20 Pubchem ID :21363
Synonyms :
Chemical Name :Cyclohexylacetic acid

Calculated chemistry of [ 5292-21-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.23
TPSA : 37.3 ?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) : -5.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.7
Log Po/w (XLOGP3) : 2.26
Log Po/w (WLOGP) : 2.04
Log Po/w (MLOGP) : 1.57
Log Po/w (SILICOS-IT) : 1.65
Consensus Log Po/w : 1.84

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.01
Solubility : 1.38 mg/ml ; 0.0097 mol/l
Class : Soluble
Log S (Ali) : -2.68
Solubility : 0.297 mg/ml ; 0.00209 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.07
Solubility : 12.1 mg/ml ; 0.0851 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.5

Safety of [ 5292-21-7 ]

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 [ 5292-21-7 ]

* 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 [ 5292-21-7 ]

[ 5292-21-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1189-71-5 ]
  • [ 5292-21-7 ]
  • [ 4435-14-7 ]
YieldReaction ConditionsOperation in experiment
14.6 g (85%) In dichloromethane; N,N-dimethyl-formamide; Step (1) Preparation of Cyclohexylacetonitrile A solution of the cyclohexylacetic acid (20.0 g, 141 mmol) in CH2 Cl2 (80 mL) was heated to reflux and a solution of chlorosulfonyl isocyanate (20.9 g, 148 mmol) in CH2 Cl2 (18 mL) was added dropwise over 40 minutes. After the addition was complete, stirring was continued at reflux for 65 minutes. The mixture was cooled to 0 C., and DMF (21.1 g, 288 mmol) was added dropwise. The mixture was allowed to warm to room temperature and stirred 18 hours. The mixture was poured over ice, the organic layer separated, and the aqueous layer extracted with CH2 Cl2 (50 mL). The combined organic layers were washed with water (3*50 mL), brine, dried (Na2 SO4), filtered through a plug of Florosil and concentrated. The nitrile was obtained as 14.6 g (85%) of an oil of sufficient purity for use in the next reaction. NMR (DMSO-d6, 200 MHz): delta 1.10 (m, 5H), 1.62 (m, 6H), 2.40 (d, J=7.0, 2H).
  • 2
  • [ 5292-21-7 ]
  • [ 4435-14-7 ]
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