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35666-77-4

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35666-77-4 Usage

General Description

(S)-3-Methylhexanoic acid is a compound with the chemical formula C7H14O2. It is a carboxylic acid with a branched structure and a specific stereochemistry, denoted by the "S" in its name. (S)-3-METHYLHEXANOIC ACID is used in various industries, including food, pharmaceuticals, and cosmetics. It is known for its fruity and cheesy odor, making it a common ingredient in flavoring and fragrance applications. Additionally, it is also used as a precursor in the synthesis of other organic compounds. The presence of the methyl group in its structure gives it unique properties that make it suitable for a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 35666-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,6 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35666-77:
(7*3)+(6*5)+(5*6)+(4*6)+(3*6)+(2*7)+(1*7)=144
144 % 10 = 4
So 35666-77-4 is a valid CAS Registry Number.

35666-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-METHYLHEXANOIC ACID

1.2 Other means of identification

Product number -
Other names CYCLOHEXANONE,3-METHYL

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:35666-77-4 SDS

35666-77-4Relevant articles and documents

Method for the Production of Optically Active 3-Alkyl Carboxylic Acids and the Intermediate Products Thereof

-

, (2008/06/13)

An enantioselective method for producing optically active 3-alkyl carboxylic acids comprises transforming an optically active secondary alcohol into an optically active, activated compound by introducing a leaving group; reacting the activated compound with a malonic acid derivative to obtain an optically active, alkylated malonic acid compound, the reaction taking place exclusively in ether and/or carboxylic acid ester solvents and one or more aprotic polar solvents or alcohols as a cosolvent in a maximum proportion of 30 volume percent of total solvent, wherein the added cosolvent is not hexamethyl phosphoric acid triamide; the malonic acid compound is hydrolyzed if necessary to obtain the corresponding acid; and the corresponding acid is decarboxylated.

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