40432-40-4 Usage
Uses
Used in Pharmaceutical Industry:
1-Benzyl-azetidine-2-carboxylic acid amide is used as a building block in organic synthesis for the preparation of various pharmaceuticals and biologically active compounds due to its unique structure and functional groups.
Used in Antidepressant and Analgesic Applications:
In the field of medicinal chemistry, 1-benzyl-azetidine-2-carboxylic acid amide is used as an antidepressant and analgesic agent, offering potential therapeutic benefits for the treatment of mood disorders and pain management.
Used in Antimicrobial and Antifungal Applications:
1-BENZYL-AZETIDINE-2-CARBOXYLIC ACID AMIDE is also utilized as an antimicrobial and antifungal agent, providing a means to combat various microbial infections and fungal pathogens.
Used in Anticancer Research:
1-Benzyl-azetidine-2-carboxylic acid amide has shown potential as a potent inhibitor of protein tyrosine phosphatase 1B, which is an important target for the development of new antidiabetic drugs, thus it is used in the research and development of novel cancer therapeutics.
Used in Medicinal Chemistry Research:
As a promising lead compound, 1-benzyl-azetidine-2-carboxylic acid amide is extensively used in medicinal chemistry research for exploring its various biological activities and potential applications in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 40432-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40432-40:
(7*4)+(6*0)+(5*4)+(4*3)+(3*2)+(2*4)+(1*0)=74
74 % 10 = 4
So 40432-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O/c12-11(14)10-6-7-13(10)8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H2,12,14)
40432-40-4Relevant academic research and scientific papers
Enzymatic resolution of methyl N-alkyl-azetidine-2-carboxylates by Candida antarctica lipase-mediated ammoniolysis
Starmans, Wim A. J.,Doppen, Roy G.,Thijs, Lambertus,Zwanenburg, Binne
, p. 429 - 435 (2007/10/03)
A facile method for the synthesis of optically active azetidine-2- carboxylic acid derivatives is presented Racemic N-alkylated azetidine esters are resolved by lipase from Candida antarctica in an ammoniolysis reaction, and both the S-amide and the R-ester are obtained with excellent stereoselectivity.
