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Butyric acid, 3-(carboxyamino)-, 3-ethyl ester (7CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91928-95-9

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91928-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91928-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,2 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91928-95:
(7*9)+(6*1)+(5*9)+(4*2)+(3*8)+(2*9)+(1*5)=169
169 % 10 = 9
So 91928-95-9 is a valid CAS Registry Number.

91928-95-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxycarbonylamino-buttersaeure

1.2 Other means of identification

Product number -
Other names 3-Ethoxycarbonylamino-butyric acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91928-95-9 SDS

91928-95-9Downstream Products

91928-95-9Relevant academic research and scientific papers

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

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Paragraph 0027; 0030, (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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