33567-53-2 Usage
General Description
Methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is a chemical compound that belongs to the class of oxirane derivatives. It is commonly used as an intermediate in organic synthesis and pharmaceutical manufacturing. It is a colorless liquid with a sweet, fruity odor, and is soluble in organic solvents. methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate is known for its versatile reactivity and is used in a wide range of applications, including the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure makes it a valuable building block for the synthesis of various complex organic molecules, making it a valuable tool in chemical research and development.
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 articles and documents
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.
Substituted aralkyl aldehydes: preparation and antitumor evaluation.
Billman,Tonnis
, p. 1188 - 1192 (2007/10/11)
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