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Benzeneacetic acid, a-[[(2-nitrophenyl)thio]amino]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16679-41-7

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16679-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16679-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,7 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16679-41:
(7*1)+(6*6)+(5*6)+(4*7)+(3*9)+(2*4)+(1*1)=137
137 % 10 = 7
So 16679-41-7 is a valid CAS Registry Number.

16679-41-7SDS

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 N-<(o-nitrophenyl)sulfenyl>-D-phenylglycine

1.2 Other means of identification

Product number -
Other names (R)-(2-Nitro-phenylsulfanylamino)-phenyl-acetic acid

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:16679-41-7 SDS

16679-41-7Downstream Products

16679-41-7Relevant academic research and scientific papers

High potency dipeptide sweeteners. 1. L-aspartyl-D-phenylglycine esters

Janusz,Gardklik,Young,Burkes,Stoll,Estelle,Riley

, p. 1052 - 1061 (2007/10/02)

Twenty esters of L-aspartyl-D-phenylglycine, as well as two substituted analogues, an o-fluoro and a p-hydroxyphenylglycine ester, were prepared. The L-aspartyl-D-phenylglycine (-)-α- and (+)-β-fenchyl esters had the highest sweetness potency at 1200 and 3700 times that of sucrose, respectively. The high potency of these sweeteners is surprising as the phenyl group occupies a position previously believed to accommodate only much smaller groups.

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