7729-30-8 Usage
Description
D-Azetidine-2-carboxylic acid is a four-membered ring analog of L-Proline, an essential amino acid. It possesses unique structural properties due to its cyclic nature, which makes it a valuable compound in various chemical and pharmaceutical applications.
Uses
Used in Pharmaceutical Industry:
D-Azetidine-2-carboxylic acid is used as a key intermediate in the synthesis of polypeptides for pharmaceutical applications. Its unique cyclic structure allows for the development of novel peptide-based drugs with improved stability and bioactivity.
Used in Chemical Synthesis:
D-Azetidine-2-carboxylic acid is used as a versatile building block in the synthesis of various organic compounds. Its four-membered ring structure provides a unique platform for the development of new chemical entities with potential applications in various industries.
Used in Research and Development:
D-Azetidine-2-carboxylic acid is utilized in research and development for the study of peptide conformation, protein folding, and enzyme mechanisms. Its unique properties enable researchers to gain insights into the fundamental aspects of peptide chemistry and biology.
Check Digit Verification of cas no
The CAS Registry Mumber 7729-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7729-30:
(6*7)+(5*7)+(4*2)+(3*9)+(2*3)+(1*0)=118
118 % 10 = 8
So 7729-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2/c6-4(7)3-1-2-5-3/h3,5H,1-2H2,(H,6,7)/t3-/m1/s1
7729-30-8Relevant articles and documents
Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates
Ma, Sang-ho,Yoon, Doo Ha,Ha, Hyun-Joon,Lee, Won Koo
, p. 269 - 271 (2007/10/03)
Enantiopure 1-phenylethylazetidine-2-carboxylates and 2-acylazetidines were prepared and reacted with chloroformates to yield α-chloro-γ-amino butyric acid esters and ketones from ring opening reaction of azetidinium ion intermediate in a completely regio- and stereoselective manner.
3-Pyridyl enantiomers and their use as analgesics
-
, (2008/06/13)
The present invention relates to a method of controlling pain in mammals, including humans, comprising administering to a mammal or patient in need of treatment thereof selected compounds of formula I: STR1 or a pharmaceutically acceptable salt thereof. The invention further relates to selected (R) and (S) compounds of formula I above which are useful as analgesics as well as neuronal cell death preventors and anti-inflammatories.
