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ethyl [(4S,5R)-4,5-diphenyloxazolidin-2-on-3-yl]acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1147849-07-7

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1147849-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1147849-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,8,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1147849-07:
(9*1)+(8*1)+(7*4)+(6*7)+(5*8)+(4*4)+(3*9)+(2*0)+(1*7)=177
177 % 10 = 7
So 1147849-07-7 is a valid CAS Registry Number.

1147849-07-7Relevant academic research and scientific papers

A practical synthesis of enantiopure 4,4,4-trifluoro-allo-threonine from an easily available fluorinated building block

Cho, Joonil,Irie, Siho,Iwahashi, Nobutaka,Itoh, Yoshimitsu,Saigo, Kazuhiko,Ishida, Yasuhiro

, p. 127 - 131 (2015)

A practical method to prepare enantiopure 4,4,4-trifluoro-allo-threonine was developed by using an easily available fluorinated building block and a chiral auxiliary as starting materials. Trifluoroacetic anhydride was annulated with a ketene, derived fro

CARBACEPHEM BETA-LACTAM ANTIBIOTICS

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Page/Page column 57-58, (2010/04/06)

Carbacephem β-lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, X, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM β-LACTAM ANTIBIOTICS

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Page/Page column 61-62, (2010/04/06)

Carbacephem -lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar1, Ar2, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM BETA-LACTAM ANTIBIOTICS

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Page/Page column 51-52, (2010/11/05)

Carbacephem β-lactam antibiotics having chemical structures (I) and (II) are disclosed: including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R6 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM β-LACTAM ANTIBIOTICS

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Page/Page column 75-76, (2009/05/30)

Carbacephem β-lactam antibiotics having the following chemical structures (I) and (II) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R3 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

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