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2-methyl-1-vinyl-1H-imidazole is a chemical compound characterized by its molecular formula C6H7N3 and a molar mass of 109.14 g/mol. It is a yellow to light brown liquid at room temperature, exhibiting slight solubility in water. 2-methyl-1-vinyl-1H-imidazole is recognized for its polymerization and crosslinking capabilities with other monomers, which underpins its significance in various industrial applications.

2851-95-8

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2851-95-8 Usage

Uses

Used in Polymer Synthesis:
2-methyl-1-vinyl-1H-imidazole is utilized as a monomer in the synthesis of polymers, particularly specialty polymers. Its ability to polymerize and crosslink with other monomers is crucial for creating materials with unique properties tailored for specific applications.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-methyl-1-vinyl-1H-imidazole is employed as a key component in the development of new drugs. Its chemical properties allow for the creation of novel drug molecules with potential therapeutic benefits.
Used in Agrochemicals:
2-methyl-1-vinyl-1H-imidazole is also used in the production of agrochemicals, where it may contribute to the formulation of pesticides, herbicides, or other agricultural products that require stable and effective chemical compounds.
Used in Adhesives and Coatings:
2-methyl-1-vinyl-1H-imidazole finds application in the manufacturing of adhesives and coatings, where its polymerization properties can enhance the durability, bonding strength, and protective qualities of these products.
Used in Electronics:
2-methyl-1-vinyl-1H-imidazole is employed in the electronics industry, potentially for the development of materials used in semiconductors, circuit boards, or other electronic components that require specific chemical and physical properties.
Overall, 2-methyl-1-vinyl-1H-imidazole is a versatile compound with applications spanning across various industries, highlighting its importance in the realm of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 2851-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2851-95:
(6*2)+(5*8)+(4*5)+(3*1)+(2*9)+(1*5)=98
98 % 10 = 8
So 2851-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2/c1-3-8-5-4-7-6(8)2/h3-5H,1H2,2H3

2851-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-2-methylimidazole

1.2 Other means of identification

Product number -
Other names N-Vinyl-2-methylimidazole

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:2851-95-8 SDS

2851-95-8Relevant academic research and scientific papers

Flocculation of a synthetic rubber latex with homopolymers and copolymers of N-vinylcaprolactam and N-vinylimidazoles

Shatalov,Verezhnikov,Churilina,Kuznetsov,Poyarkova

, p. 1839 - 1843 (2003)

Flocculation of a latex of SKS-30 ARK commercial rubber with homopolymers and copolymers of N-vinylcaprolactam, 1-vinyl-2-methylimidazole, and its quaternization product was studied. The flocculating power of the nonionic polymers in acid solution was evaluated. The performance of the copolymers grows with increasing content of cationic units in the macromolecules and on adding an acid.

Separating material

-

, (2008/06/13)

The present invention provides a separating material producable by a) providing a solid substrate, having amino-functional groups coupled to the substrate surface, b) covalently coupling of the amino-functional groups with a thermally labile radical initiator, c) contacting the substrate surface with a solution of polymerizable monomers under conditions, where thermally initiated graft copolymerization of the monomers takes place, to form a structure of adjacent functional polymer chains on the surface of the substrate. The present invention further provides a method for the production of a separating material by a) providing a solid substrate, having amino-functional groups coupled to the substrate surface, b) covalently coupling of the amino-functional groups with a thermally labile radical initiator, c) contacting the substrate surface with a solution of polymerizable monomers under conditions, where thermally initiated graft copolymerization of the monomers takes place, to form a structure of adjacent functional polymer chains on the surface of the substrate.

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