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6974-87-4

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6974-87-4 Usage

General Description

ETHYL A-BROMOLAURATE is a chemical compound with the molecular formula C12H23BrO2. It is an ester of lauric acid and is commonly used in the production of various cosmetic and personal care products such as soaps, shampoos, and lotions. It is also used as a fragrance ingredient and as a flavoring agent in food products. Ethyl A-Bromolaurate is known for its pleasant, fruity aroma and is considered safe for use in cosmetics and food products when used in accordance with regulations and guidelines. Additionally, it is often used as an intermediate in the synthesis of other organic compounds due to its versatile chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6974-87-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6974-87:
(6*6)+(5*9)+(4*7)+(3*4)+(2*8)+(1*7)=144
144 % 10 = 4
So 6974-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H27BrO2/c1-3-5-6-7-8-9-10-11-12-13(15)14(16)17-4-2/h13H,3-12H2,1-2H3

6974-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL A-BROMOLAURATE

1.2 Other means of identification

Product number -
Other names 2-Brom-dodecansaeure-aethylester

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:6974-87-4 SDS

6974-87-4Relevant articles and documents

Unnatural nucleosides and nucleotides. III. Preparation of 2-14C and 4-14C labelled 5-alkyluracils and 5-alkyl-2'-deoxyuridines

Szabolcs,Kruppa,Sagi,Otvos

, p. 713 - 726 (2007/10/08)

2-14C Labelled 5-alkyluracils were prepared by condensation of the diethylacetals of α-formyl-carbonic acid esters with 14C-thiourea. Compounds labelled at 4-C were synthesized by condensation of the labelled carboxylic acid derivatives with thiourea. β-Anomers of 5-alkyl-2'-deoxyuridines were obtained in a fairly good radiochemical yield. Alkyl substituents ranged from methyl to tetradecyl, isopropyl and tert-butyl.

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