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(5R,2R)-2,5-Diaminoadipic acid 2HCl is a chemical compound that is the 2HCl salt of (5R,2R)-2,5-diaminoadipic acid, a derivative of the essential amino acid lysine. It is widely used in organic synthesis and as a biochemical reagent, offering added stability and solubility due to its 2HCl salt form, making it suitable for various applications in the pharmaceutical and chemical industries.

213686-08-9

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213686-08-9 Usage

Uses

Used in Pharmaceutical Industry:
(5R,2R)-2,5-Diaminoadipic acid 2HCl is used as a key intermediate in the synthesis of drug molecules and medicinal compounds, contributing to the development of new pharmaceuticals.
Used in Chemical Research and Development:
(5R,2R)-2,5-Diaminoadipic acid 2HCl is utilized as a biochemical reagent in the research and development of new chemical compounds and materials, facilitating advancements in the chemical industry.

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 academic research and scientific papers

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

Stereospecific synthesis of cyclic hydrazoacetic acids and meso- diaminodicarboxylic acids

Arakawa, Yasushi,Goto, Takahiro,Kawase, Kazuya,Yoshifuji, Shigeyuki

, p. 674 - 680 (2007/10/03)

The hetero Diels-Alder adducts 6a - d derived from azodibenzoyl and cyclic dienes were oxidized by ruthenium tetroxide and transformed into meso- diaminodicarboxylic acids 12a - d via the new cyclic hydrazoacetic acids 9a - d.

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