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cis-1-benzoylmethyl-3-phenoxyacetamido-4-phenylazetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114497-99-3

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114497-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114497-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114497-99:
(8*1)+(7*1)+(6*4)+(5*4)+(4*9)+(3*7)+(2*9)+(1*9)=143
143 % 10 = 3
So 114497-99-3 is a valid CAS Registry Number.

114497-99-3Downstream Products

114497-99-3Relevant academic research and scientific papers

PYRIDINE ASSISTED OXIDATIONS OF ALCOHOLS TO CARBONYL COMPOUNDS BY MEANS OF 3-CARBOXYPYRIDINIUM DICHROMATE (NDC) REAGENT.

Cossio, Fernando P.,Lopez, Concepcion M.,Palomo, Claudio

, p. 3963 - 3974 (2007/10/02)

3-carboxypyridinium dichromate (NDC), readly prepareted from nicotinic acid and chromium trioxide, is an efficient reagent for the oxidation of alcohols into carbonyl compounds in the presence of pyridine.The optimum molar ratio substrate:reagent:pyridine to ensure complete oxidation of starting material in a short reaction time was found 1:2.5:20 respectlively.A brief compouison between this reagent and pyridinium dichromate (PDC) is made.In contrast to the PDC reagent, NDC allows selective oxidation between benzylic alcohols and aliphatic alcohols.The NDC-pyridine system has been successfully extended to the oxidation of N-(2-hidroxy-2-phenyl or 2-methylethyl)-β-lactams into their corresponding carbonyl compounds as N-H azetidin-2-one precursor.In contrast, primary N-(2-hydroxyethyl)-β-lactams upon treatment with this reagent system afforded N-formylazetidin-2-ones.The influence of pyridine in oxidations by means of NDC is further shown in the conversion of hydroquinones into quinones.Another interesting feature associated with the use of this reagent is the ease of purification of the final products.

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