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1140737-02-5

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1140737-02-5 Usage

General Description

(S)-2-Aminooct-7-enoic acid is a chemical compound also known as (S)-(E)-2-Amino-7-octenoic acid. It is an amino acid with a unique structure containing a double bond in its side chain. (S)-2-Aminooct-7-enoic acid is not commonly found in nature, and its biological functions are still being studied. However, it has been identified as a potential component of certain bacterial and fungal metabolites. The presence of the double bond in its side chain may give it distinct chemical properties and biological activities compared to other amino acids, making it an interesting target for further research in the field of organic chemistry and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1140737-02-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,0,7,3 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1140737-02:
(9*1)+(8*1)+(7*4)+(6*0)+(5*7)+(4*3)+(3*7)+(2*0)+(1*2)=115
115 % 10 = 5
So 1140737-02-5 is a valid CAS Registry Number.

1140737-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-aminooct-7-enoic acid

1.2 Other means of identification

Product number -
Other names I04-1450

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:1140737-02-5 SDS

1140737-02-5Upstream product

1140737-02-5Downstream Products

1140737-02-5Relevant articles and documents

Novel preparation of chiral α-amino acids using the Mitsunobu-Tsunoda reaction

Noisier, Anais F. M.,Harris, Craig S.,Brimble, Margaret A.

supporting information, p. 7744 - 7746 (2013/09/02)

An efficient synthesis of racemic or optically active α-amino acids by modified-Mitsunobu alkylation of a racemic or chiral glycine template from alcohols was developed. Libraries of amino acids were prepared in moderate to good yield with good to high enantioselectivity. This simple method widens the scope for preparation of structurally diverse amino acids.

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