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213686-08-9

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213686-08-9 Usage

General Description

(5R,2R)-2,5-Diaminoadipic acid 2HCl is a chemical compound consisting of 2HCl salt of (5R,2R)-2,5-diaminoadipic acid. It is a derivative of the essential amino acid lysine and is commonly used in organic synthesis and as a biochemical reagent. (5R,2R)-2,5-Diaminoadipic acid 2HCl is often utilized in the production of pharmaceuticals, particularly in the synthesis of drug molecules and medicinal compounds. Additionally, it is also used in the research and development of new chemical compounds and materials. The 2HCl salt form of (5R,2R)-2,5-diaminoadipic acid provides added stability and solubility, making it suitable for various applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 213686-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 213686-08:
(8*2)+(7*1)+(6*3)+(5*6)+(4*8)+(3*6)+(2*0)+(1*8)=129
129 % 10 = 9
So 213686-08-9 is a valid CAS Registry Number.

213686-08-9SDS

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 (5R,2R)-2,5-Diaminoadipic acid 2HCl

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:213686-08-9 SDS

213686-08-9Downstream Products

213686-08-9Relevant articles and documents

Synthesis of (2S,5S)-5-fluoromethylornithine; a potent inhibitor of ornithine aminotransferase

Ducep,Heintzelmann,Jund,Lesur,Schleimer,Zimmermann

, p. 327 - 335 (1997)

Only one of the four enantiomers of 5-fluoromethylornithine 1 was an irreversible inhibitor of ornithine aminotransferase. The active enantiomer la was synthesized from diaminoadipic acid 2 with a chemical diastereomeric separation and an enantiomeric res

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