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164175-55-7

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164175-55-7 Usage

Chemical category

Maleimides

Common use

Crosslinking agent in polymerization and material science applications

Structure

Two maleimide groups separated by a 2-methyl-pentane spacer

Bonding ability

Forms stable and strong covalent bonds with thiol-containing molecules

Applications

Adhesives, coatings, and biocompatible polymers

Reactivity

High

Stability

High

Field of use

Materials science and chemical engineering

Check Digit Verification of cas no

The CAS Registry Mumber 164175-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,1,7 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 164175-55:
(8*1)+(7*6)+(6*4)+(5*1)+(4*7)+(3*5)+(2*5)+(1*5)=137
137 % 10 = 7
So 164175-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2O4/c1-10(9-16-13(19)6-7-14(16)20)3-2-8-15-11(17)4-5-12(15)18/h4-7,10H,2-3,8-9H2,1H3

164175-55-7SDS

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 1-[5-(2,5-dioxopyrrol-1-yl)-4-methylpentyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:164175-55-7 SDS

164175-55-7Downstream Products

164175-55-7Relevant articles and documents

AMIDE-EXTENDED CROSSLINKING COMPOUNDS AND METHODS FOR USE THEREOF

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Page/Page column 64, (2010/04/03)

The invention is based on the discovery that a remarkable improvement in the performance of maleimide thermosets can be achieved by incorporating amide-extended maleimides into an adhesive formulation. Amide-extended maleimides described herein can be used to toughen bismaleimide thermosetting materials without sacrificing any thermal stability. Amide-extended maleimides are readily prepared by reacting a bismaleimide with an appropriate amine via the well-known Michael addition reaction. Acylation of the resulting secondary amines provides the amide-extended maleimide. The acylating agent can also be used to introduce polymerizable functional groups into the backbones of these thermoset monomers. Amide-extended acrylate and methacrylate monomers can also be prepared.

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