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S-[2-[3-[[4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] prop-2-enethioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5776-58-9

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5776-58-9 Usage

Uses

Acrylyl-CoA can be used to determine clinical, biochemical, and genetic features of patients with short-chain enoyl-coA hydratase (ECHS1) deficiency. It can also be used to prepare fluorescent probe-based reactome array for detecting, immobilizing and isolating enzymes.

Definition

ChEBI: The S-acryloyl derivative of coenzyme A.

Check Digit Verification of cas no

The CAS Registry Mumber 5776-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5776-58:
(6*5)+(5*7)+(4*7)+(3*6)+(2*5)+(1*8)=129
129 % 10 = 9
So 5776-58-9 is a valid CAS Registry Number.

5776-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name acryloyl-CoA

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:5776-58-9 SDS

5776-58-9Relevant academic research and scientific papers

On the thermodynamic equilibrium between (R)-2-hydroxyacyl-CoA and 2-enoyl-CoA

Parthasarathy, Anutthaman,Buckel, Wolfgang,Smith, David M.

experimental part, p. 1738 - 1746 (2011/04/18)

A combined experimental and computational approach has been applied to investigate the equilibria between several α-hydroxyacyl-CoA compounds and their 2-enoyl-CoA derivatives. In contrast to those of their β, γ and α counterparts, the equilibria for the α-compounds are relatively poorly characterized, but qualitatively they appear to be unusually sensitive to substituents. Using a variety of techniques, we have succeeded in measuring the equilibrium constants for the reactions beginning from 2-hydroxyglutaryl-CoA and lactyl-CoA. A complementary computational evaluation of the equilibrium constants shows quantitative agreement with the measured values. By examining the computational results, we arrive at an explanation of the substituent sensitivity and provide a prediction for the, as yet unmeasured, equilibrium involving 2-hydroxyisocaproyl-CoA.

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