1384745-48-5 Usage
Description
(S)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester is a chemical compound with the molecular formula C15H21NO2. It is a derivative of azetidine, featuring a four-membered heterocyclic ring with one nitrogen atom, a benzyl group, and a methyl ester functional group. (S)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester's chiral center enables the synthesis of enantiopure compounds, making it a valuable intermediate in drug development and chemical research.
Uses
Used in Pharmaceutical Industry:
(S)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester is used as a chiral building block for the preparation of various pharmaceuticals and bioactive compounds. Its unique structure and chiral center allow for the creation of enantiopure compounds, which are essential in the development of new drugs and bioactive molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester serves as an important intermediate. Its structural features and functional groups facilitate the synthesis of complex molecules with potential therapeutic applications, contributing to the advancement of drug discovery and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 1384745-48-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,7,4 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1384745-48:
(9*1)+(8*3)+(7*8)+(6*4)+(5*7)+(4*4)+(3*5)+(2*4)+(1*8)=195
195 % 10 = 5
So 1384745-48-5 is a valid CAS Registry Number.
1384745-48-5Relevant articles and documents
Practical preparation of enantiopure 2-methyl-azetidine-2-carboxylic acid; a γ-turn promoter
Drouillat, Bruno,Wright, Karen,Marrot, Jerome,Couty, Francois
, p. 690 - 696 (2012/09/21)
A robust and practical synthesis of each enantiomer of 2-methyl-azetidine- 2-carboxylic acid, based on the use of (S)-phenylglycinol as resolving agent, is described. This synthesis affords practical quantities of this quaternary amino acid suitably N- an
