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77582-61-7

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77582-61-7 Usage

General Description

Heneicosanoyl chloride is a type of fatty acid derived compound that is commonly used in organic synthesis. It belongs to the family of long-chain fatty acyl chlorides and is specifically derived from heneicosanoic acid, a 21-carbon fatty acid. Heneicosanoyl chloride is used as a reagent in various chemical reactions to introduce the heneicosanoyl group into organic molecules, such as in the formation of esters and amides. It is a colorless to pale yellow liquid with a strong, pungent odor and is known to be corrosive and highly reactive. Overall, heneicosanoyl chloride plays a significant role in organic chemistry as a versatile compound for creating complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 77582-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,8 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77582-61:
(7*7)+(6*7)+(5*5)+(4*8)+(3*2)+(2*6)+(1*1)=167
167 % 10 = 7
So 77582-61-7 is a valid CAS Registry Number.

77582-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name henicosanoyl chloride

1.2 Other means of identification

Product number -
Other names HENEICOSANOYL CHLORIDE

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:77582-61-7 SDS

77582-61-7Upstream product

77582-61-7Downstream Products

77582-61-7Relevant articles and documents

Mesogenic 3,6-bis(4-hydroxyphenyl)-1,2,4,5-tetrazine alkanoate esters

Fouad, Farid,Khabouchi, Faycal,Nielsen, Alek,Twieg, Robert

, p. 82 - 90 (2019/02/24)

A novel series of 3,6-bis(4-hdroxyphenyl)-1,2,4,5-tetrazine alkanoate esters were synthesized and their mesogenic properties were studied using differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). The impact of changing the tail-core linkage from alkyl or alkoxy to ester is profound. Compared to the alkyl or alkoxy linkages, the ester linkage reduced mesogenic properties. Short-tailed compounds are non mesogenic (4a-4e), while long-tailed compounds (4f-4r) exhibit nematic phases. Unlike the alkyl or alkoxy tail series, none of the 18 presented esters in this series exhibits a smectic phase.

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