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3-Methyl-2-[3-oxo-4-(2-phenoxy-acetylamino)-3H-isothiazol-2-yl]-but-2-enoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22297-57-0

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22297-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22297-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,9 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22297-57:
(7*2)+(6*2)+(5*2)+(4*9)+(3*7)+(2*5)+(1*7)=110
110 % 10 = 0
So 22297-57-0 is a valid CAS Registry Number.

22297-57-0Downstream Products

22297-57-0Relevant academic research and scientific papers

Improved Procedure for Conversion of Penicillin V into Monocyclic β-Lactams

Davis, Michael,Wu, Wen-Yang

, p. 223 - 229 (2007/10/02)

Improved procedures for the preparation of the Kamiya compound (3R,4R)-4-(benzothiazol-2'-yldithio)-3-phenoxyacetamidoazetidin-2-one (6) from penicillin V (1) are described.A novel feature is ozonolysis, near room temperature, in aqueous methanol in the p

THE TRAPPING OF SULFENIC ACIDS FROM PENICILLIN SULFOXIDES. ARYL MERCAPTANS

Micetich, Ronald G.,Maiti, Samarendra N.,Tanaka, Motoaki,Yamazaki, Tomio,Ogawa, Kazuo

, p. 1403 - 1409 (2007/10/02)

Aryl mercaptans, unlike heterocyclic mercaptans, reacted exceptionally slowly with penicillin sulfoxides.These reactions are affected by the substituent at the C-6 position of the penam, and by the nature of the ester group at the C-3 position.The unsym- azetidinone disulfides obtained from these reactions, unlike those from heterocyclic mercaptans, did not react with halogenating agents such as cupric chloride.

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