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116070-49-6

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116070-49-6 Usage

General Description

2,2-Dimethyl-malonamic acid is a chemical compound with the molecular formula C6H9NO4. It is a derivative of malonamic acid and contains two methyl groups. 2,2-DIMETHYL-MALONAMIC ACID is often used as a building block in organic synthesis and pharmaceutical research. It has been studied for its potential application in the field of medicine and drug development. 2,2-Dimethyl-malonamic acid has shown promise as a ligand in metal complexation and has been utilized in the development of chiral catalysts for various chemical reactions. Additionally, it has been investigated for its potential use in the synthesis of bioactive compounds and pharmaceutical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 116070-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116070-49:
(8*1)+(7*1)+(6*6)+(5*0)+(4*7)+(3*0)+(2*4)+(1*9)=96
96 % 10 = 6
So 116070-49-6 is a valid CAS Registry Number.

116070-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-2,2-dimethyl-3-oxopropanoic acid

1.2 Other means of identification

Product number -
Other names 2,2-DIMETHYL-MALONAMIC ACID

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:116070-49-6 SDS

116070-49-6Relevant articles and documents

Unusual Formation of New Indole-Containing Heterocyclic Ring System

Black, David St. C.,Chaichit, Narongsak,Gatehouse, Bryan M.,Moss, G. Ian

, p. 1965 - 1977 (2007/10/02)

The oxazinoindoletrione (3) underwent reaction with aqueous ammonia in methanol or ethanol to yield the polycyclic methyl or ethyl esters (4) and (5) respectively.Reaction of trione (3) with gaseous ammonia in dry ethanol gave the aminobenzodiazepinone (7).This compound lost ammonia on heating in toluene to give compound (11) and in the presence of methanol or ethanol gave the methyl or ethyl esters (9) and (10) respectively.The structures of compounds (4), (7) and (10) were all established by X-ray crystallography.

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