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13893-43-1

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13893-43-1 Usage

General Description

"(R)-2-AMINO-PENTANOIC ACID ETHYL ESTER" is a chemical compound with the molecular formula C7H15NO2. It is also known by the chemical name ethyl (R)-2-aminopentanoate. (R)-2-AMINO-PENTANOIC ACID ETHYL ESTER is a chiral building block that is commonly used in the pharmaceutical industry for the synthesis of various pharmaceutical products. It is known to exhibit biological activity and has been used as a precursor in the preparation of enantiomerically pure drugs. Additionally, it has been studied for its potential use in organic chemistry and medicinal chemistry research. (R)-2-AMINO-PENTANOIC ACID ETHYL ESTER has potential applications in the development of new drugs and other biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 13893-43-1 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 13893-43:
(7*1)+(6*3)+(5*8)+(4*9)+(3*3)+(2*4)+(1*3)=121
121 % 10 = 1
So 13893-43-1 is a valid CAS Registry Number.

13893-43-1SDS

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-aminopentanoate

1.2 Other means of identification

Product number -
Other names -

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:13893-43-1 SDS

13893-43-1Relevant articles and documents

Efficient synthesis of α-substituted amino acid ester: Alkylation and hydrogenation removal of Schiff's base protecting group

Ansari, Aslam M.,Ugwu, Sydney O.

, p. 2330 - 2340 (2008)

A general and efficient synthetic route to α-amino acids by alkylation of the sodium salt of Schiff base ester 1 has been described previously. The α-substituted ethyl glycinates 4a-g are prepared in excellent yield by a two-step sequence involving regios

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Hauser,Reynolds

, p. 4250 (1948)

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The use of alpha-amino acids in the synthesis of derivatives of 2-aminoethanethiol as potential antiradiation agents.

Piper,Stringfellow Jr.,Johnston

, p. 911 - 920 (2007/10/05)

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