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Allyl hydrogen maleate, with the molecular formula C5H6O4, is an ester of maleic acid and allyl alcohol. It is a clear, colorless liquid with a strong odor and is highly reactive due to the presence of the allyl group. This chemical compound is commonly used in the synthesis of polymers and resins.

2424-58-0

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2424-58-0 Usage

Uses

Used in Polymer and Resin Synthesis:
Allyl hydrogen maleate is used as a monomer for the production of various thermosetting plastics, adhesives, and coatings. Its reactivity and ability to cross-link with other molecules make it a valuable component in these applications.
Used in Automotive Coatings and Composites:
In the automotive industry, allyl hydrogen maleate is used as a cross-linking agent to enhance the durability and performance of coatings and composites. Its inclusion in these products contributes to improved resistance to wear, weathering, and other environmental factors.
Safety Precautions:
It is important to handle allyl hydrogen maleate with care, as it can be a skin and eye irritant. Additionally, it has the potential to form explosive peroxides when exposed to air, so proper storage and handling procedures must be followed to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 2424-58-0 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 2424-58:
(6*2)+(5*4)+(4*2)+(3*4)+(2*5)+(1*8)=70
70 % 10 = 0
So 2424-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O4/c1-2-5-11-7(10)4-3-6(8)9/h2-4H,1,5H2,(H,8,9)/b4-3-

2424-58-0SDS

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 allyl maleate

1.2 Other means of identification

Product number -
Other names (Z)-3-(allyloxycarbonyl) acrylic 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:2424-58-0 SDS

2424-58-0Relevant academic research and scientific papers

COMPOUNDS AND METHODS FOR THE TREATMENT OF CYSTIC FIBROSIS

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Page/Page column 60-61, (2020/08/22)

The invention relates to a compound of Formula I, pharmaceutical compositions comprising a compound of Formula I, and pharmaceutically acceptable slats thereof, pharmaceutical compositions comprising such compounds and methods of treating cystic fibrosis comprising the step of administering a therapeutically effective amount of a compound of Formula I to a subject in need thereof.

APAF-1 INHIBITOR COMPOUNDS

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Page/Page column 7, (2012/05/21)

Derivatives of 2,5-piperazinedione of formula (I) are apoptotic peptidase activating factor 1 (Apaf-1) inhibitors, therefore they are useful as active pharmaceutical ingredients for the prophylaxis and/or treatment of a pathological and/or physiological condition associated with an increase of apoptosis.

COMPOUND THAT CAN INHIBIT UBC13-UEV INTERACTIONS, PHARMACEUTICAL COMPOSITIONS AND THERAPEUTIC USES

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Page/Page column 31-41, (2009/04/23)

The invention relates to a compound (I) wherein R is a heterocyclyl radical; R1 and R2 are independently H or alkyl; R3 is H, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, aryl, arylalkyl, heterocyclyl or heterocyclylalkyl; R4 and R5 are independently H or alkyl; q is a number selected from 0 and 1; and the salts, solvates, prodrugs or stereoisomers thereof having inhibitory activity for UBC13-UEV interactions and which can be used in the production of pharmaceutical compositions intended for antitumor therapy or the treatment and/or prophylaxis of diseases associated to metabolic pathways involving the UBC13 enzyme, metabolic pathways involving transcriptional factor NF-κB, or pathways involving PCNA or RAD6. ????????R- (CR1R2) q-CO-N (R3)-C(R4R5)-CO-NH2?????(I)

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