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151144-96-6

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151144-96-6 Usage

General Description

L-2-AMINO-4-BROMO-4-PENTENOIC ACID is an organic compound with the molecular formula C5H8BrNO2. It is a derivative of the amino acid lysine and contains a bromine atom and a pentenoic acid group. L-2-AMINO-4-BROMO-4-PENTENOIC ACID is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its chemical structure and properties make it useful in the development of potential drug candidates and in the production of crop protection products. L-2-AMINO-4-BROMO-4-PENTENOIC ACID has potential applications in the fields of medicine and agriculture, making it a significant chemical in the research and development of new compounds for these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 151144-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,1,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 151144-96:
(8*1)+(7*5)+(6*1)+(5*1)+(4*4)+(3*4)+(2*9)+(1*6)=106
106 % 10 = 6
So 151144-96-6 is a valid CAS Registry Number.

151144-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-4-bromopent-4-enoic acid

1.2 Other means of identification

Product number -
Other names AL562-1

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:151144-96-6 SDS

151144-96-6Relevant articles and documents

Highly diastereoselective monoalkylation and Michael addition of N- (diphenylmethylene)glycinesultam under solid-liquid phase-transfer catalysis conditions using potassium carbonate as base

Lopez, Anna,Pleixats, Roser

, p. 1967 - 1977 (2007/10/03)

Treatment of a sultam-derived N-(diphenylmethylene)glycinate equivalent 1 with activated (allylic and propargylic) organic bromides and with Michael acceptors under solid-liquid phase-transfer catalysis conditions, using potassium carbonate as base, affords the monoalkylated compounds with high diastereoselectivity (>97% d.e.).

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