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phenyl hydrogen maleate ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38013-07-9

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38013-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38013-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38013-07:
(7*3)+(6*8)+(5*0)+(4*1)+(3*3)+(2*0)+(1*7)=89
89 % 10 = 9
So 38013-07-9 is a valid CAS Registry Number.

38013-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl hydrogen maleate ester

1.2 Other means of identification

Product number -
Other names Maleinsaeure-monophenylester

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:38013-07-9 SDS

38013-07-9Relevant academic research and scientific papers

Structure-activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A)

Van Veldhoven,Blad,Artsen,Klopman,Wolfram,Abdelkadir,Lane,Brussee,Ijzerman

supporting information; experimental part, p. 2736 - 2739 (2011/06/20)

Nicotinic acid (niacin) has been used for decades as an antidyslipidemic drug in man. Its main target is the hydroxy-carboxylic acid receptor HCA2 (GPR109A), a G protein-coupled receptor. Other acids and esters such as methyl fumarate also interact with the receptor, which constituted the basis for the current study. We synthesized a novel series of substituted propenoic acids, such as fumaric acid esters, fumaric acid amides and cinnamic acid derivatives, and determined their affinities for the HCA2 receptor. We observed a rather restricted binding pocket on the receptor with trans-cinnamic acid being the largest planar ligand in our series with appreciable affinity for the receptor. Molecular modeling and analysis of the structure-activity relationships in the series suggest a planar trans-propenoic acid pharmacophore with a maximum length of 8 ? and out-of-plane orientation of the larger substituents.

Kinetic and theoretical studies on the mechanism of intramolecular catalysis in phenyl ester hydrolysis

Andres, Gabriel O.,Pierini, Adriana B.,De Rossi, Rita H.

, p. 7650 - 7656 (2007/10/03)

(Chemical Equation Presented) The kinetic study of the hydrolysis reaction of Z-substituted phenyl hydrogen maleates (Z = H, m-CH3, p-CH 3, m-Cl, p-Cl and m-CN) was carried out in aqueous solution, and the results were complemented with theoretical studies. Under some experimental conditions, two kinetic processes were observed. One of them was ascribed to maleic anhydride formation and the other to the anhydride hydrolysis. The Broensted-type plot for the leaving-group dependence was linear with slope βlg = -1. The experimental results are consistent with a mechanism that involves significant bond breaking in the rate-limiting transition state (αlg = 0.64). Theoretical results for the reaction in the gas phase showed an excellent Broensted-type dependence with a βlg of -1.03. A tetrahedral intermediate (TI) could not be found through DFT gas-phase studies (B3LYP/6-311+G*). Calculations carried out within a continuous solvation model or with discrete water molecules failed to find a stable TI. With both models, a flat region on the potential-energy surface is found and a tight optimization of the structures led back to starting materials. The theoretical results do not discard the possible existence of an unstable intermediate on the free-energy surface, but the analysis of the whole body of results compared with other acyl transfer reactions lead us to suggest that an enforced concerted mechanism is the most appropriate to describe these reactions.

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