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71101-89-8

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71101-89-8 Usage

General Description

4-Butylcyclohexane carboxylic acid, also known as 4-butylcyclohexanecarboxylic acid, is a chemical compound with the molecular formula C11H20O2. It is a carboxylic acid that belongs to the class of cycloalkanes, which are hydrocarbons with a closed ring structure. 4-Butylcyclohexane carboxylic acid is commonly used as a pharmaceutical intermediate in the synthesis of various drugs. It is also used as a building block in the production of other organic compounds. 4-Butylcyclohexane carboxylic acid has a variety of applications in the pharmaceutical and chemical industries, and its unique structure makes it a valuable starting material for the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 71101-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,0 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71101-89:
(7*7)+(6*1)+(5*1)+(4*0)+(3*1)+(2*8)+(1*9)=88
88 % 10 = 8
So 71101-89-8 is a valid CAS Registry Number.

71101-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BUTYLCYCLOHEXANE CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 4-(4-BUTYLCYCLOHEXYL)BENZONITRILE

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:71101-89-8 SDS

71101-89-8Relevant articles and documents

Epimerization of 2- or 4- substituted cyclohexanecarboxylic acids

-

, (2008/06/13)

The present invention relates to a new method for obtaining a purity of about 93% to 100% of the trans form of 2- or 4-substituted cyclohexanecarboxylic acid or reactive derivatives thereof from the cis form or a mixture of the cis and trans forms by a single step, particularly, to a method for obtaining a purity of substantially 100% of the trans form of 4-substituted cyclohexanecarboxylic acid.

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