108957-96-6 Usage
General Description
N-isopropyl-N-methylglycine, also known as sarcosine, is a natural amino acid derivative with the chemical formula C3H7NO2. It is a non-proteinogenic amino acid, meaning it is not involved in the synthesis of proteins in the body. Sarcosine is involved in several biological processes, including the metabolism of choline and production of creatine. It has also been studied for its potential therapeutic effects in the treatment of mental health disorders, such as schizophrenia, depression, and anxiety. Additionally, sarcosine has been investigated for its role in cancer metabolism and prognosis. Overall, N-isopropyl-N-methylglycine has multiple functions in the body and holds promise for various medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 108957-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108957-96:
(8*1)+(7*0)+(6*8)+(5*9)+(4*5)+(3*7)+(2*9)+(1*6)=166
166 % 10 = 6
So 108957-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-5(2)7(3)4-6(8)9/h5H,4H2,1-3H3,(H,8,9)
108957-96-6Relevant articles and documents
Photolysis of Tertiary Amines in the Presence of CO2: The Paths to Formic Acid, α-Amino Acids, and 1,2-Diamines
Berton, Mateo,Mello, Rossella,Acerete, Rafael,González Núnez, María Elena
, p. 96 - 103 (2018)
The photolysis of triethylamine (1a) in the presence of carbon dioxide leads to the hydrogenation of CO2, the α-C-C coupling of 1a, and the CO2 insertion into the α-C-H σ-bond of amine 1a. This reaction is proposed to proceed through the radical ion pair [R3N?+·CO2?-] generated by the photoionization of amine 1a and the electron capture by CO2. The presence of lithium tetrafluoroborate in the reaction medium promotes the efficient and stereoselective α-C-C coupling of 1a by enhancing the production of α-dialkylamino radicals and the isomerization of N,N,N′,N′-tetraethylbutane-2,3-diamine (4a).