33912-39-9 Usage
General Description
1-(4-chlorophenyl)-4-phenylazetidin-2-one is a chemical compound with the molecular formula C15H12ClNO. It is a lactam compound that belongs to the azetidinone class and contains a chlorine atom attached to a phenyl ring. This chemical compound has been studied for its potential pharmacological properties, particularly its anti-inflammatory and analgesic effects. It may also have application in the field of organic synthesis and medicinal chemistry. Its structure and properties make it a potential candidate for the development of new pharmaceutical drugs and biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 33912-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,1 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33912-39:
(7*3)+(6*3)+(5*9)+(4*1)+(3*2)+(2*3)+(1*9)=109
109 % 10 = 9
So 33912-39-9 is a valid CAS Registry Number.
33912-39-9Relevant articles and documents
Copper-Catalyzed Oxidative Benzylic C(sp3)?H Cyclization for the Synthesis of β-Lactams
Nozawa-Kumada, Kanako,Saga, Satoshi,Matsuzawa, Yuta,Hayashi, Masahito,Shigeno, Masanori,Kondo, Yoshinori
, p. 4496 - 4499 (2020/04/10)
β-Lactams are important structural motifs because of their ubiquity in natural products and pharmaceuticals. We report herein a Cu-catalyzed intramolecular oxidative C(sp3)?H amidation for the synthesis of β-lactams using tBuOOtBu. This method
Synthesis and Stereochemistry of 3-(α-Hydroxybenzyl)-1,4-diphenyl-2-azetidinones
Otto, Hans-Hartwig,Mayrhofer, Roswitha,Bergmann, Hans-Joachim
, p. 1152 - 1161 (2007/10/02)
Aldol reaction between benzaldehydes and 1,4-diphenyl-2-azetidinones 1 catalyzed by lithium diisopropylamide results in formation of the title compound The reactions give satisfactory yields and high diastereoselectivity at three centres in forming the αS
