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ETHYL 2-AMINO-2-METHYLPENTANOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13893-47-5

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13893-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13893-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13893-47:
(7*1)+(6*3)+(5*8)+(4*9)+(3*3)+(2*4)+(1*7)=125
125 % 10 = 5
So 13893-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2/c1-4-6-8(3,9)7(10)11-5-2/h4-6,9H2,1-3H3

13893-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 2-AMINO-2-METHYLPENTANOATE

1.2 Other means of identification

Product number -
Other names ethyl 2-azanyl-2-methyl-pentanoate

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:13893-47-5 SDS

13893-47-5Downstream Products

13893-47-5Relevant academic research and scientific papers

BENZAMIDINE DERIVATIVES SUBSTITUTED BY AMINO ACID AND HYDROXY ACID DERIVATIVES AND THEIR USE AS ANTI-COAGULANTS

-

, (2008/06/13)

This invention is directed to benzamidine derivatives substituted by amino acid and hydroxy acid derivatives which are useful as anti-coagulants. This invention is also directed to pharmaceutical compositions containing the compounds of the invention, and methods of using the compounds to treat disease-states characterized by thrombotic activity.

The asymmetric synthesis of allylglycine and other unnatural α-amino acid via zinc-mediated allylation of oximes in aqueous media

Hanessian, Stephen,Yang, Rui-Yang

, p. 5273 - 5276 (2007/10/03)

Enantiomerically pure or highly enriched allylglycine and its chain-substituted analogs are easily accessible from the reaction of the sultam derivative of O-benzyl glyoxylic acid oxime with allylic bromides in the presence of powdered zinc in aqueous ammonium chloride.

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