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3-[(ethoxycarbonyl)amino]-3-phenylpropanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93136-45-9

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93136-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93136-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93136-45:
(7*9)+(6*3)+(5*1)+(4*3)+(3*6)+(2*4)+(1*5)=129
129 % 10 = 9
So 93136-45-9 is a valid CAS Registry Number.

93136-45-9Relevant academic research and scientific papers

Synthetic method for beta-amino acids and beta-amino acids synthesized by adopting method

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, (2018/03/25)

The invention relates to a novel synthetic method for beta-amino acids and the beta-amino acids synthesized by adopting the method. The method comprises the following steps: an amide and an azo diacidester are taken as raw materials, an intermediate compound I is synthesized through direct carbon-hydrogen bond amination under the action of a catalyst, the intermediate compound I reacts with methyl bromoacetate to synthesize an intermediate compound II, an amide protecting group is removed under acidic conditions, and therefore the beta-amino acid is obtained; and the chemical structural formula of the beta-amino acid obtained by synthesis is shown in the description, wherein in a formula, R1 and R2 are separately one selected from the group consisting of hydrogen, alkyl, branched alkyl, cycloalkyl, aryl, aryl with various substituents, a heterocyclic group and a heterocyclic group with various substituents; and R3 is an ester group. Compared with the prior art, the method provided bythe invention synthesizes the intermediate compound I through the direct carbon-hydrogen bond amination process, so that substrates can be broadened in a wide range, the synthesized beta-amino acids with substituents in alpha and beta positions have structural diversity, and therefore the method provides a novel method for the industrialized production of the beta-amino acids with the substituentsin the alpha and beta positions.

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