7148-06-3 Usage
Description
N,N-Dimethylglycine methyl ester, also known as sarcosine methyl ester, is an organic compound with the chemical formula C4H9NO2. It is a derivative of dimethylglycine, an amino acid found in proteins, and is characterized by the presence of a methyl ester functional group. N,N-DIMETHYLGLYCINE METHYL ESTER is known for its potential applications in various fields, including pharmaceuticals, biochemistry, and chemical research.
Uses
Used in Proteomics Research:
N,N-Dimethylglycine methyl ester is used as a biochemical for proteomics research. It serves as a valuable tool in the study of protein structure, function, and interactions, contributing to a better understanding of biological processes and the development of novel therapeutic strategies.
Used as a Chemical Intermediate:
N,N-Dimethylglycine methyl ester is also utilized as a chemical intermediate in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique chemical properties make it a versatile building block for the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N-Dimethylglycine methyl ester is used as an intermediate for the synthesis of drugs targeting various medical conditions. Its role in the development of new therapeutic agents highlights its importance in the advancement of healthcare solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 7148-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7148-06:
(6*7)+(5*1)+(4*4)+(3*8)+(2*0)+(1*6)=93
93 % 10 = 3
So 7148-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-6(2)4-5(7)8-3/h4H2,1-3H3
7148-06-3Relevant articles and documents
Substituent Effects on the Product Distribution in Diazo Amide Photochemistry. Role of Ground-State Conformational Populations
Tomioka, Hideo,Kondo, Masato,Izawa, Yasuji
, p. 1090 - 1094 (2007/10/02)
Effects of substituents on the photochemical processes of several α-diazo amides (1a-f) have been studied .Irradiation of 1b in ethyl ether and acetone afforded, in addition to a β-lactam, the reaction products with the solvents, ie., EtOCH2CONMe2 and 1,3-dioxolane, respectively, whereas similar irradiation of 1a in these solvents gave only intramolecular reaction products, ie., β- and γ-lactams.Displacement of oneof the alkyl groups on the amide nitrogen with a Ph group markedly changed its photochemical processes.Thus irradiations of 1c and 1d in MeOH gave oxindole almost exclusively.Introduction of an acetyl group on the diazo carbon also caused a change in the product distributions.Photolysis of 1e in methanol gave, for exaple, the Wolff rearrangement (WR) product of Me migration and a β-lactam, whereas similar irradiation of 1f afforded WR product and oxindole.The results are interpreted as indicating that the β-lactam, the oxindole, and the WR product are derived from the excited singlet state of s-Z form of the diazo amide itself, whereas that of s-E form dissociates nitrogen to generate singlet carbene, and that populations of each conformers in the ground state are important in determining the photochemical processes of the α-diazo amide.