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(S)-3-((3S,4R)-1-Benzyl-2-oxo-4-phenyl-azetidin-3-yl)-4-phenyl-oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99333-59-2

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99333-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99333-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99333-59:
(7*9)+(6*9)+(5*3)+(4*3)+(3*3)+(2*5)+(1*9)=172
172 % 10 = 2
So 99333-59-2 is a valid CAS Registry Number.

99333-59-2Downstream Products

99333-59-2Relevant academic research and scientific papers

Triphosgene: A versatile reagent for the synthesis of azetidin-2-ones

Krishnaswamy,Govande,Gumaste,Bhawal,Deshmukh

, p. 2215 - 2225 (2007/10/03)

An efficient use of triphosgene, as an acid activator, for the synthesis of substituted azetidin-2-ones via ketene-imine cycloaddition reaction using various acids and imines have been described.

The asymmetric synthesis of β-lactam antibiotics. I. Application of chiral oxazolidones in the Staudinger Reaction

Evans,Sjogren

, p. 3783 - 3786 (2007/10/02)

The reactions of oxazolidone with N-benzylimines proceed with exceptional levels of asymmetric induction to form the cycloadducts. Subsequent dissolving metal reduction affords the homochiral β-lactam derivatives in good overall yield.

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