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Methacryloyl isocyanate, with the molecular formula C6H7NO2, is a chemical compound that serves as a versatile building block in the synthesis of various materials. It is known for its reactivity with a range of compounds, including alcohols, amines, and thiols, which allows it to form stable bonds. This characteristic, coupled with its ability to undergo polymerization reactions, makes it a valuable component in the production of polymers, resins, acrylics, adhesives, and coatings. Despite its utility, methacryloyl isocyanate is toxic and can cause irritation to the skin, eyes, and respiratory system, thus requiring careful handling and safety measures during its application.

4474-60-6

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4474-60-6 Usage

Uses

Used in Polymer and Resin Production:
Methacryloyl isocyanate is used as a monomer in the production of polymers and resins for its ability to readily react with other compounds, contributing to the formation of stable and versatile materials.
Used in Acrylics and Coatings:
In the acrylics and coatings industry, methacryloyl isocyanate is used as a reactive component to enhance the properties of the final products, such as durability and chemical resistance.
Used in Adhesives:
Methacryloyl isocyanate is used as a key ingredient in adhesive formulations to improve adhesion strength and create bonds that are resistant to various environmental conditions.
Used in Specialty Coatings and Adhesives Development:
Methacryloyl isocyanate is utilized as a reactive building block in the development of specialty coatings and adhesives that possess unique properties tailored for specific applications, such as high-strength bonding or resistance to harsh chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 4474-60-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4474-60:
(6*4)+(5*4)+(4*7)+(3*4)+(2*6)+(1*0)=96
96 % 10 = 6
So 4474-60-6 is a valid CAS Registry Number.

4474-60-6SDS

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 2-methylprop-2-enoyl isocyanate

1.2 Other means of identification

Product number -
Other names 2-Propenoyl isocyanate,2-methyl

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:4474-60-6 SDS

4474-60-6Relevant academic research and scientific papers

Method of preparing acylisocyanates

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, (2008/06/13)

The invention relates to a novel process for the preparation of acyl isocyanates which consists in reacting oxalyl chloride with an N-trialkylsilylcarboxamide or an N,N-bis(trialkylsilyl)carboxamide. The process makes it possible to obtain acyl isocyanates in good yield, in particular acyl isocyanates derived from aliphatic amides, and under simplified reaction conditions.

Process for the preparation of acyl isocyanates

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, (2008/06/13)

The invention concerns a process for the preparation of acyl isocyanates which consists of reacting oxalyl chloride with a salt selected from the group consisting of hydrohalides and sulphates of carboxamides and/or carbamates, unsubstituted on nitrogen, then heating the reaction mixture at a temperature between 30° and 150° C. The process is suitable for preparation of acyl isocyanates with excellent yields in easy to control operational conditions.

Production of isocyanate compounds

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, (2008/06/13)

Production of an alkenoyl isocyanate of the formula: STR1 wherein R is a hydrogen atom or a lower alkyl group by reacting an acrylamide of the formula: STR2 wherein R is as defined above with an oxalyl halide of the formula(COX) 2wherein X is a halogen at

Preparation of alkenoyl isocyanates

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, (2008/06/13)

A process for preparing alkenoyl isocyanates of the formula: STR1 wherein R is a hydrogen atom or a lower alkyl group which comprises subjecting an oxazolinedione hydrohalide of the formula: STR2 wherein X is a halogen atom and R is as defined above to decomposition under an ordinary pressure, in the presence of a hydrogen halide-eliminating agent and/or in a liquid medium having a dielectric constant of not more than 4.

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