33567-53-2 Usage
Uses
Used in Pharmaceutical Manufacturing:
Methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is used as an intermediate in the production of pharmaceuticals for its versatile reactivity and ability to be a building block for complex organic molecules.
Used in Agrochemical Production:
Methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is used as an intermediate in the production of agrochemicals, contributing to the development of effective and innovative products in this industry.
Used in Specialty Chemicals Synthesis:
Methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is used as an intermediate in the synthesis of specialty chemicals, providing a wide range of applications across various industries.
Used in Chemical Research and Development:
Methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is used as a valuable tool in chemical research and development due to its unique structure and reactivity, enabling the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 33567-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,6 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33567-53:
(7*3)+(6*3)+(5*5)+(4*6)+(3*7)+(2*5)+(1*3)=122
122 % 10 = 2
So 33567-53-2 is a valid CAS Registry Number.
33567-53-2Relevant academic research and scientific papers
Dynamic kinetic asymmetric transformations of β-halo-α-keto esters by N,N′-dioxide/Ni(II)-catalyzed carbonyl-ene reaction
Liu, Wen,Cao, Weidi,Hu, Haipeng,Lin, Lili,Feng, Xiaoming
supporting information, p. 8901 - 8904 (2018/08/17)
Dynamic kinetic asymmetric transformations of racemic β-halo-α-keto esters through carbonyl-ene reaction were realized using a chiral N,N′-dioxide-nickel(ii) complex, giving the corresponding β-halo-α-hydroxy esters containing two vicinal chiral tri- and tetrasubstituted carbon centers in good yields and dr with excellent ee values without the use of extra bases. Meanwhile, a proposed reaction mechanism was presented according to the configuration of the product.
STEREOSPECIFIC PREPARATION OF TRANS-GLYCIDIC ESTERS
Polniaszek, Richard P.,Belmont, Stephen E.
, p. 221 - 232 (2007/10/02)
Trans-disubstituted glycidic esters have been prepared stereospecifically by reaction of the dicyclopentylborylenolate of α-bromo-t-butylthioacetate with aromatic aldehydes.
