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Cyclohexanol, 4-(1,1-dimethylethyl)-1-ethenyl-, cis- is a chemical compound with the molecular formula C11H20O. It is a cyclic alcohol with a cyclohexane ring structure, featuring a 1-ethenyl (vinyl) group and a 1,1-dimethylethyl (tert-butyl) group at the 4-position. The cis-configuration indicates that the substituents are on the same side of the double bond. Cyclohexanol, 4-(1,1-dimethylethyl)-1-ethenyl-, cis- is an organic compound with potential applications in the synthesis of various chemicals, pharmaceuticals, and materials due to its unique structure and reactivity.

7103-35-7

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7103-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7103-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,0 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7103-35:
(6*7)+(5*1)+(4*0)+(3*3)+(2*3)+(1*5)=67
67 % 10 = 7
So 7103-35-7 is a valid CAS Registry Number.

7103-35-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Vinyl-cis-4-tert.-butyl-cyclohexanol

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-1-vinyl-cyclohexanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7103-35-7 SDS

7103-35-7Relevant academic research and scientific papers

Novel Conversion of Epoxides to One Carbon Homologated Allylic Alcohols by Dimethylsulfonium Methylide

Alcaraz, L.,Harnett, J. J.,Mioskowski, C.,Martel, J. P.,Gall, T. Le,et al.

, p. 5449 - 5452 (2007/10/02)

The reaction of excess of dimethylsulfonium methylide with terminal, allylic, or benzylic epoxides affords good to excellent yields of one carbon homologated allylic alcohols.

STEREOCHEMICAL OUTCOME OF THE REACTION OF SOME α-SELENOALKYLLITHIUMS WITH 4-t-BUTYL CYCLOHEXANONE

Labar, D.,Krief, A.,Norberg, B.,Evrard, G.,Durant, F.

, p. 1083 - 1100 (2007/10/02)

α-selenoalkyllithiums were found to have a high propensity to add to 4-t-butyl cyclohexanone in an equatorial mode.Stereochemical assignments are discussed.

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