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Nonanedioic acid, 2-amino, dimethyl ester, hydrochloride is a chemical compound with the molecular formula C11H23NO4.HCl. It is an organic compound derived from nonanedioic acid, which is a dicarboxylic acid with a nine-carbon chain. The 2-amino group indicates the presence of an amino group attached to the second carbon atom in the chain. The dimethyl ester part of the name signifies that the carboxylic acid groups are esterified with two methyl groups. The hydrochloride (HCl) indicates that the compound is a salt formed by the reaction of the parent compound with hydrochloric acid. Nonanedioic acid, 2-amino-, dimethyl ester, hydrochloride is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and other organic compounds. It is important to handle Nonanedioic acid, 2-amino-, dimethyl ester, hydrochloride with care due to its potential reactivity and sensitivity to moisture.

5722-16-7

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5722-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5722-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5722-16:
(6*5)+(5*7)+(4*2)+(3*2)+(2*1)+(1*6)=87
87 % 10 = 7
So 5722-16-7 is a valid CAS Registry Number.

5722-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-aminononanedioate,hydrochloride

1.2 Other means of identification

Product number -
Other names Nonanedioic acid,2-amino-,dimethyl ester,hydrochloride

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:5722-16-7 SDS

5722-16-7Relevant academic research and scientific papers

Methotrexate analogues. 34. Replacement of the glutamate moiety in methotrexate and aminopterin by long-chain 2-aminoalkanedioic acids

Rosowsky,Bader,Kohler,Freisheim,Moran

, p. 1338 - 1344 (1988)

Eight previously unreported methotrexate (MTX) and aminopterin (AMT) analogues with the L-glutamate moiety replaced by DL-2-aminoalkanedioic acids containing up to 10 CH2 groups were synthesized from 4-amino-4-deoxy-N10-methylpteroic

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