913814-30-9 Usage
Description
Azetidine, 1-(diphenylMethyl)-3-phenylis a chemical compound with the molecular formula C23H25N. It is a cyclic amine with a five-membered ring structure, and it contains both a phenyl and diphenylmethyl group. Azetidine, 1-(diphenylMethyl)-3-phenylis commonly used as a building block in organic synthesis and has been studied for its potential pharmaceutical applications. Azetidine, 1-(diphenylMethyl)-3-phenylhas shown promising biological activities, including anticancer and antiviral properties, which make it a valuable target for further research and drug development.
Uses
Used in Pharmaceutical Industry:
Azetidine, 1-(diphenylMethyl)-3-phenylis used as a building block in organic synthesis for the development of new pharmaceutical compounds. Its unique structure and promising biological activities, such as anticancer and antiviral properties, make it a valuable target for further research and drug development.
Used in Organic Synthesis:
Azetidine, 1-(diphenylMethyl)-3-phenylis used as a key intermediate in the synthesis of various organic compounds. Its five-membered ring structure and the presence of phenyl and diphenylmethyl groups provide a versatile platform for the creation of new molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 913814-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,1 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 913814-30:
(8*9)+(7*1)+(6*3)+(5*8)+(4*1)+(3*4)+(2*3)+(1*0)=159
159 % 10 = 9
So 913814-30-9 is a valid CAS Registry Number.
913814-30-9Relevant articles and documents
Counterion-Induced Asymmetric Control in Ring-Opening of Azetidiniums: Facile Access to Chiral Amines
Qian, Deyun,Chen, Min,Bissember, Alex C.,Sun, Jianwei
, p. 3763 - 3766 (2018/03/13)
Counterion-induced stereocontrol is a powerful tool in organic synthesis. However, such enantiocontrol on tetrahedral ammonium cations remains challenging. Described here is the first example of using chiral anion phase-transfer catalysis to achieve intermolecular ring-opening of azetidiniums with excellent enantioselectivity (up to 97 % ee). Precise control over the formation and reaction of the chiral ion pair as well as inhibition of the background reaction by the biphasic system is key to the success of the reaction.
6-N-Linked Heterocycle-Substituted 2,3,4,5-Tetrahydro-1H-Benzo[d]Azepines as 5-Ht2c Receptor Agonists
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Page/Page column 21, (2008/12/08)
The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula I as selective 5-HT2C receptor agonists for the treatment of 5-HT2C associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: Formula (I) where: R6 is selected from the group consisting of (a, b, c, d, e) and other substituents are as defined in the specification.
