79731-35-4 Usage
Uses
Used in Pharmaceutical Industry:
H-GLY-DL-ASP-OH H2O is used as a building block for protein synthesis, facilitating the production of essential proteins required for various biological functions.
Used in Biochemical Research:
H-GLY-DL-ASP-OH H2O is utilized as a research tool to study the role of amino acids in protein synthesis, the urea cycle, and neurotransmission, contributing to a better understanding of these processes.
Used in Nutraceutical Industry:
H-GLY-DL-ASP-OH H2O is employed as a dietary supplement to support protein synthesis and overall health, providing the body with essential amino acids and hydration.
Used in Cosmetic Industry:
H-GLY-DL-ASP-OH H2O is used as an ingredient in skincare products to promote hydration and maintain skin health, taking advantage of its amino acid composition and water content.
Used in Food and Beverage Industry:
H-GLY-DL-ASP-OH H2O is utilized as a flavor enhancer and a source of essential amino acids in various food and beverage products, improving taste and nutritional value.
Check Digit Verification of cas no
The CAS Registry Mumber 79731-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,3 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79731-35:
(7*7)+(6*9)+(5*7)+(4*3)+(3*1)+(2*3)+(1*5)=164
164 % 10 = 4
So 79731-35-4 is a valid CAS Registry Number.
79731-35-4Relevant articles and documents
Regulating morphologies and near-infrared photothermal conversion of perylene bisimide: Via sequence-dependent peptide self-assembly
Cui, Lingyun,Jiao, Yang,Wang, Anhe,Zhao, Luyang,Dong, Qianqian,Yan, Xuehai,Bai, Shuo
supporting information, p. 2208 - 2211 (2018/03/06)
The assembly behavior of perylene bisimide (PBI) can be precisely organised by the conjugation of sequence-dependent di-peptides in aqueous media. The assembled nanostructures and consequent properties of PBI aggregates can be tuned by the use of differen
Mild Conversion of Carboxamides and Carboxylic Acid Hydrazides to Acids and Esters
Greenlee, William J.,Thorsett, Eugene D.
, p. 5351 - 5353 (2007/10/02)
A mild and selective conversion of unsubstituted carboxamides and carboxylic acid hydrazides to the corresponding acids and esters is brought about by the use of acidic resins.Application of the procedure to several carboxamides and carboxylic acid hydrazides is described.