40327-51-3 Usage
Description
(4-methoxyphenyl)(3-phenyloxiran-2-yl)methanone is a chemical compound utilized as a fundamental building block in the realm of organic synthesis. This versatile ketone is characterized by the presence of a methoxyphenyl group and a phenyloxiran-2-yl group, which significantly contribute to the compound's reactivity and distinctive properties. Its unique structure and reactivity render it a promising candidate for the development of novel pharmaceuticals, agrochemicals, and an array of other fine chemicals.
Uses
Used in Pharmaceutical Industry:
(4-methoxyphenyl)(3-phenyloxiran-2-yl)methanone is employed as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drugs with potential applications in treating a wide range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (4-methoxyphenyl)(3-phenyloxiran-2-yl)methanone is used as a vital component in the development of innovative agrochemicals. Its incorporation into these products can lead to enhanced efficacy and targeted action against pests and diseases, ultimately contributing to improved crop yields and food security.
Used in Organic Chemistry:
(4-methoxyphenyl)(3-phenyloxiran-2-yl)methanone also serves as a versatile intermediate for the synthesis of a diverse array of compounds in organic chemistry. Its unique reactivity and structural features make it an invaluable tool for researchers and chemists working on the development of new materials and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 40327-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,2 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40327-51:
(7*4)+(6*0)+(5*3)+(4*2)+(3*7)+(2*5)+(1*1)=83
83 % 10 = 3
So 40327-51-3 is a valid CAS Registry Number.
40327-51-3Relevant articles and documents
A high-yielding protocol for the synthesis of 4,5-diarylpyrimidin-2-amine derivatives from chalcones
Kooramatom Unni, Krishnaraj,Menon, Prasanth K.,George, Scholly Clair,Thomas, Sajesh P.,Devaky
, p. 112 - 118 (2021/10/07)
A novel, high yielding and versatile protocol was achieved for the synthesis of 4,5-diaryl-2-pyrimidinamine derivatives from chalcones. The synthesis was accomplished by converting the chalcones into 3-chloro-2,3-diaryl-2-propen-1-ones followed by subsequent reaction with amidine derivatives.
Asymmetric epoxidation of α,β-unsaturated ketones catalyzed by rare-earth metal amides RE[N(SiMe3)2]3with chiral TADDOL ligands
Shan, Haiwen,Lu, Chengrong,Zhao, Bei,Yao, Yingming
, p. 1043 - 1053 (2021/01/25)
The catalytic asymmetric epoxidation of α,β-unsaturated ketones by tert-butylhydroperoxide (TBHP) has been well established using rare-earth metal amides RE[N(SiMe3)2]3 (RE = La(1), Nd(2), Sm(3), Y(4), Yb(5)) with chiral TADDOL ligands. It was found that
Ligand regulation for manganese-catalyzed enantioselective epoxidation of olefins without acid
Xu, Daqian,Sun, Qiangsheng,Lin, Jin,Sun, Wei
supporting information, p. 13101 - 13104 (2020/11/09)
A novel manganese catalyst bearing an l-proline-derived N4 ligand has been developed for enabling acid-free asymmetric epoxidation of olefins with tert-butyl hydroperoxide as the oxidant. A variety of olefins that are well-matched in size with the ligand
