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octyl N-chloro-2-methylalaninate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59660-97-8

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59660-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59660-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59660-97:
(7*5)+(6*9)+(5*6)+(4*6)+(3*0)+(2*9)+(1*7)=168
168 % 10 = 8
So 59660-97-8 is a valid CAS Registry Number.

59660-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name octyl 2-(chloroamino)-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names Alanine,N-chloro-2-methyl-,octyl 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:59660-97-8 SDS

59660-97-8Downstream Products

59660-97-8Relevant academic research and scientific papers

N-chloro-amino acid derivatives activity

-

, (2008/06/13)

There is provided, a novel class of compounds exhibiting antibacterial activity, said compounds having the formula: EQU1 wherein X and Y each represent a member which may be the same or different selected from the group consisting of H and Cl with the pri

N halo derivatives III: Stabilization of nitrogen chlorine bond in N chloroamino acid derivatives

Kaminski,Bodor,Higuchi

, p. 553 - 557 (2007/10/05)

The chlorination of α amino acids and their related derivatives was investigated. A kinetic study of the stability of these N chlorinated products led to an elucidation of the factors that significantly influence the stability and research of the nitrogen chlorine bond in these N chloramines. From the kinetic investigations, a series of low chlorine potential, soft antimicrobial N chloramines was developed based on derivatives of α aminoisobutyric acid and related compounds.

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