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124703-69-1

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124703-69-1 Usage

General Description

Methyl 3-aminoacrylate is a chemical compound that has the molecular formula C4H7NO2. It is a highly reactive and versatile molecule that is commonly used in organic synthesis and as a building block for various pharmaceuticals and agrochemicals. It is also commonly used in the production of adhesives and as a monomer for various polymers. Methyl 3-aminoacrylate has a wide range of applications in the chemical industry due to its ability to undergo various chemical reactions and form stable compounds with different functional groups. However, it is important to handle this compound with caution as it can be potentially hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 124703-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124703-69:
(8*1)+(7*2)+(6*4)+(5*7)+(4*0)+(3*3)+(2*6)+(1*9)=111
111 % 10 = 1
So 124703-69-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2/c1-7-4(6)2-3-5/h2-3H,5H2,1H3/b3-2+

124703-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-aminoprop-2-enoate

1.2 Other means of identification

Product number -
Other names Methyl 3-aminoacrylate

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:124703-69-1 SDS

124703-69-1Downstream Products

124703-69-1Relevant articles and documents

A structure-reactivity relationship for base-promoted hydrolysis and methanolysis of monocyclic β-lactams

Rao,More O'Ferrall

, p. 2729 - 2735 (2007/10/02)

A structure-reactivity relationship for base hydrolysis and methanolysis of nearly 50 azetidinones ranging in reactivity over nine powers of 10 is described. Substituents at 3- and 4-positions show similar effects upon reactivity and are correlated by a T