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7476-81-5

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7476-81-5 Usage

General Description

(4-chlorophenyl) butanoate is a chemical compound that belongs to the family of butanoate esters. It is also known as ethyl 4-chlorophenylbutanoate and is commonly used as a fragrance and flavoring agent in the food and beverage industry. This chemical is a colorless to pale yellow liquid with a sweet, floral odor and is soluble in alcohol and oils. It is often used in the production of perfumes, cosmetics, and various food products as a flavoring agent. Additionally, (4-chlorophenyl) butanoate is also used in the manufacturing of pharmaceuticals and other industrial applications. However, it is important to handle this chemical with care, as it can be harmful if it comes into contact with the skin or is ingested.

Check Digit Verification of cas no

The CAS Registry Mumber 7476-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7476-81:
(6*7)+(5*4)+(4*7)+(3*6)+(2*8)+(1*1)=125
125 % 10 = 5
So 7476-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-2-3-10(12)13-9-6-4-8(11)5-7-9/h4-7H,2-3H2,1H3

7476-81-5SDS

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 (4-chlorophenyl) butanoate

1.2 Other means of identification

Product number -
Other names Butyric acid,p-chlorophenyl ester

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:7476-81-5 SDS

7476-81-5Relevant articles and documents

Enzymatic resolution, desymmetrization, and dynamic kinetic asymmetric transformation of 1,3-cycloalkanediols

Fransson, Ann-Britt L.,Xu, Yongmei,Leijondahl, Karin,Baeckvall, Jan-E.

, p. 6309 - 6316 (2007/10/03)

An efficient desymmetrization of cis-1,3-cyclohexanediol to (1S,3R)-3-(acetoxy)-1-cyclohexanol ((R,S)-2a) was performed via Candida antarctica lipase B (CALB)-catalyzed transesterification, in high yield (up to 93%) and excellent enantioselectivity (ee's

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