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Cyclohexyl hydrogen maleate, with the molecular formula C7H10O4, is a maleic acid derivative and a member of the cycloalkene class of cyclic organic compounds. It is a chemical compound that plays a significant role in various industrial applications due to its unique properties.

2424-59-1

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2424-59-1 Usage

Uses

Used in Polymer Production:
Cyclohexyl hydrogen maleate is used as a key component in the production of various polymer materials. Its chemical structure allows it to contribute to the formation of polymers with specific properties, making it valuable in this application.
Used in Organic Synthesis:
As a reagent, cyclohexyl hydrogen maleate is utilized in organic synthesis processes. Its ability to participate in chemical reactions facilitates the creation of a range of organic compounds, broadening its utility in the chemical industry.
Used in Manufacturing of Resins, Adhesives, and Coatings:
Cyclohexyl hydrogen maleate is employed as a raw material in the manufacturing of resins, adhesives, and coatings. Its inclusion in these products enhances their performance characteristics, such as adhesion, durability, and resistance to environmental factors.
Used in Pharmaceutical Development:
Cyclohexyl hydrogen maleate is used as an intermediate in the development of pharmaceuticals. Its role in the synthesis of drug compounds makes it an important component in the pharmaceutical industry, contributing to the creation of new medications.
Used in Chemical Production:
As an intermediate, cyclohexyl hydrogen maleate is also used in the production of other chemicals. Its versatility in chemical reactions allows it to be a part of various chemical synthesis processes, expanding its applications across different sectors.
Safety and Environmental Considerations:
It is crucial to handle cyclohexyl hydrogen maleate with care due to its potential to cause skin and eye irritation. Additionally, respiratory irritation may occur if the compound is inhaled. There is also a need to manage its environmental impact, as it can have harmful effects on aquatic organisms if released into the environment. Proper safety measures and disposal methods should be implemented to mitigate these risks.

Check Digit Verification of cas no

The CAS Registry Mumber 2424-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2424-59:
(6*2)+(5*4)+(4*2)+(3*4)+(2*5)+(1*9)=71
71 % 10 = 1
So 2424-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c11-9(12)6-7-10(13)14-8-4-2-1-3-5-8/h6-8H,1-5H2,(H,11,12)/b7-6-

2424-59-1SDS

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 cyclohexyl maleate

1.2 Other means of identification

Product number -
Other names Maleinsaeure-monocyclohexylester

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:2424-59-1 SDS

2424-59-1Relevant 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.

Benzylamine narcotic antagonists

-

, (2008/06/13)

A process for antagonizing the pharmacologic effects of a narcotic agent in warm-blooded animals, and compositions for effecting this process are disclosed.

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