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(aR)-(4-methylcyclohexane)benzylidene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92377-88-3

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92377-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92377-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,7 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92377-88:
(7*9)+(6*2)+(5*3)+(4*7)+(3*7)+(2*8)+(1*8)=163
163 % 10 = 3
So 92377-88-3 is a valid CAS Registry Number.

92377-88-3Relevant academic research and scientific papers

Conformational and structural analysis of exocyclic olefins and ketimines by multinuclear magnetic resonance

Montalvo-Gonzalez, Ruben,Montalvo-Gonzalez, J. Ascencion,Ariza-Castolo, Armando

experimental part, p. 907 - 912 (2009/05/09)

The 1H, 13C, and 15N NMR spectra of 5 exocyclic alkenes and 15 different ketimines obtained from cyclohexanone and derivatives using benzyl bromide and primary amines - are analyzed. Relative stereochemical and preferentia

A novel method for the preparation of benzylidenecyclohexanes with high optical purity

Nakamura, Shuichi,Ogura, Takahiro,Wang, Libo,Toru, Takeshi

, p. 2399 - 2402 (2007/10/03)

The enantioselective reaction of the α-thio carbanion derived from 1-phenyl-1-(phenylthio)-1-(tributylstannyl)methane with 4-substituted cyclohexanones in the presence of bis(oxazoline)s gave the products as a diastereomeric mixture. Each diastereomer obtained had high optical purity. The reaction of the α-seleno carbanion derived from the bis(phenylseleno) acetal also showed high enantioselectivity. The stereospecific elimination of the isolated diastereomers on treatment with methanesulfonyl chloride and triethylamine afforded axially chiral benzylidenecyclohexanes with high enantioselectivities up to 99% ee.

STUDIES IN ASYMMETRIC OLEFINATIONS - THE SYNTHESIS OF ENANTIOMERICALLY PURE ALLYLIDENE, ALKYLIDENE, AND BENZYLIDENE CYCLOHEXANES

Hanessian, Stephen,Beaudoin, Serge

, p. 7655 - 7658 (2007/10/02)

Treatment of alkyl cyclohexanones with topologically unique bicyclic phosphonamides derived from the C2 symmetrical (R,R)- and (S,S)-N,N'-dimethyl 1,2-trans-cyclohexane diamine leads to enantiomerically pure allylidene and benzylidene alkylcycl

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