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(2R)-2-aminopentanedioic acid hydrochloride, also known as L-2-aminopentanedioic acid hydrochloride, is a chiral compound with the chemical formula C5H11NO4·HCl. It is a derivative of 2-aminopentanedioic acid, featuring a hydrochloride salt form, which gives it a strong acidic character. (2R)-2-aminopentanedioic acid hydrochloride is an important building block in the synthesis of various pharmaceuticals and biologically active molecules due to its unique structure, which includes a central carbon atom with four different substituents: a hydroxyl group, an amino group, a carboxyl group, and a methyl group. The (2R) configuration indicates that the molecule has a specific three-dimensional arrangement, which is crucial for its interactions with other molecules, particularly in the context of enzyme catalysis and receptor binding. Its applications span across the fields of medicine, biochemistry, and materials science, where it can be used to create complex organic molecules with specific properties and functions.

617-61-8

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617-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 617-61-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 617-61:
(5*6)+(4*1)+(3*7)+(2*6)+(1*1)=68
68 % 10 = 8
So 617-61-8 is a valid CAS Registry Number.

617-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name D-glutamic acid hydrochloride

1.2 Other means of identification

Product number -
Other names D-Glutaminsaeure

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:617-61-8 SDS

617-61-8Relevant academic research and scientific papers

Highly enantioselective synthesis of cyclic and functionalized α-amino acids by means of a chiral phase transfer catalyst

Corey,Noe, Mark C,Xu, Feng

, p. 5347 - 5350 (2007/10/03)

The chiral quaternary ammonium salt 1 serves as phase transfer catalyst for the enantioselective conversion of the glycine derivative 2 to a variety of cyclic and acyclic chiral α amino acids with enantioselectivities as high as 200:1 in alkylation and Michael addition reactions.

DESIGN OF STEREOSPECIFIC INHIBITORS FOR CRYSTAL DISSOLUTION

Shimon, L. J. W.,Zbaida, D.,Addadi, L.,Leiserowitz, L.,Lahav, M.

, p. 199 - 222 (2007/10/02)

A new class of monomeric and polymeric crystal dissolution inhibitors has been prepared taking into consideration the packing arrangements and the morphologies of organic crystals.The efficiency of these inhibitors has been demonstrated by comparative morphological studies of α-glycine and by the kinetic resolution of the racemic conglomerates of his*HCl*H2O, threonine, glu*HCl, and 2,4-sec-phenetyl-3,5-dinitrobenzoate.

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