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64298-91-5

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64298-91-5 Usage

General Description

2-AMINO-2-METHYL-4-PENTENOIC ACID, also known as AMPA, is a chemical compound that belongs to the class of amino acids and is structurally similar to glutamate. It is a non-proteinogenic amino acid that has been identified in certain marine organisms and is known to function as a potent agonist of the AMPA receptor, a subtype of ionotropic glutamate receptors. AMPA is also used as a research tool to study the pharmacology and physiology of the central nervous system, particularly in relation to excitatory neurotransmission. Additionally, it has been studied for its potential therapeutic benefits in the treatment of various neurological and psychiatric disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 64298-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64298-91:
(7*6)+(6*4)+(5*2)+(4*9)+(3*8)+(2*9)+(1*1)=155
155 % 10 = 5
So 64298-91-5 is a valid CAS Registry Number.

64298-91-5SDS

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 2-AMINO-2-METHYL-4-PENTENOIC 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

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

More Details:64298-91-5 SDS

64298-91-5Downstream Products

64298-91-5Relevant articles and documents

-

Aidene,Barbot,Miginiac

, p. 117 - 127 (2007/10/03)

A new general synthesis of C-subtituted α-aminoacids is described, using at first the regioselective reaction between α-unsaturated organozincs and N-(phenylsulfanyl)iminoesters.

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