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1432-27-5

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1432-27-5 Usage

General Description

The chemical compound "(2R)-2-[(ammonioacetyl)amino]-3-(1H-indol-3-yl)propanoate" is a derivative of the amino acid tryptophan. It is composed of an amino group attached to a carbon atom, which forms a bond with a carbonyl group and an amino group, creating a propanoate structure. Additionally, the compound features an indole group, which consists of a benzene ring fused to a pyrrole ring. (2R)-2-[(ammonioacetyl)amino]-3-(1H-indol-3-yl)propanoate may have potential applications in pharmaceuticals or biochemistry due to its structural similarity to tryptophan and its potential interactions with enzymes or receptors in biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1432-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1432-27:
(6*1)+(5*4)+(4*3)+(3*2)+(2*2)+(1*7)=55
55 % 10 = 5
So 1432-27-5 is a valid CAS Registry Number.

1432-27-5SDS

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 2-[(2-aminoacetyl)amino]-3-(1H-indol-3-yl)propanoic acid

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

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More Details:1432-27-5 SDS

1432-27-5Downstream Products

1432-27-5Relevant articles and documents

PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE SYNTHESIS. USE OF A NEW DERIVATIVE, Nin-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHAN

Kiso, Yoshiaki,Inai, Masatoshi,Kitagawa, Kouki,Akita, Tadashi

, p. 739 - 742 (2007/10/02)

The 2,2,2-trichloroethoxycarbonyl (Troc) group attached at the Nin function of tryptophan by acylation with Troc-Cl in the presence of a catalytic amount of tetra-n-butylammonium hydrogensulfate can be quantitatively removed either by cadmium dust in acetic acid or under basic conditions, e. g., hydrazine hydrate and NaOH, but is resistant to strong acidic conditions.

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