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17388-96-4

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17388-96-4 Usage

General Description

(αS)-α-Amino-6-carboxy-2-oxo-2H-pyran-3-propanoic acid, also known as aspartic acid, is a non-essential amino acid that plays a crucial role in the biosynthesis of proteins. It is classified as an α-amino acid and is one of the 20 common amino acids found in proteins. Aspartic acid is involved in various biological processes, including the production of energy, the synthesis of nucleotides, and the regulation of cell function. It is also a key component of the neurotransmitters aspartate and N-acetylaspartylglutamate, which are essential for proper brain function. Additionally, aspartic acid is utilized as a food additive and is commonly found in dietary supplements and sports drinks due to its potential role in improving athletic performance and muscle recovery.

Check Digit Verification of cas no

The CAS Registry Mumber 17388-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17388-96:
(7*1)+(6*7)+(5*3)+(4*8)+(3*8)+(2*9)+(1*6)=144
144 % 10 = 4
So 17388-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO6/c10-5(7(11)12)3-4-1-2-6(8(13)14)16-9(4)15/h1-2,5H,3,10H2,(H,11,12)(H,13,14)/t5-/m0/s1

17388-96-4SDS

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 5-[(2S)-2-amino-2-carboxyethyl]-6-oxopyran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names stizolbinic 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:17388-96-4 SDS

17388-96-4Upstream product

17388-96-4Downstream Products

17388-96-4Relevant articles and documents

A biomimetic synthesis of stizolobinic acid

Baldwin, Jack E.,Spyvee, Mark R.,Whitehead, Roger C.

, p. 2771 - 2774 (2007/10/03)

Stizolobinic acid (1) was synthesized in a biomimetic fashion from an analogue of L-DOPA via an oxidative cleavage reaction.

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