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39763-02-5

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39763-02-5 Usage

Type of compound

Maleimide derivative

Common uses

Production of polymers, crosslinking proteins

Known for

Ability to react with thiol groups

Useful for

Creating stable protein conjugates and hydrogels

Utilized in

Development of advanced materials (adhesives, coatings, resins)

Studied for

Potential applications in drug delivery systems and tissue engineering

Role

Crucial in various scientific and industrial fields due to versatile chemical properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 39763-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,6 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39763-02:
(7*3)+(6*9)+(5*7)+(4*6)+(3*3)+(2*0)+(1*2)=145
145 % 10 = 5
So 39763-02-5 is a valid CAS Registry Number.

39763-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[10-(2,5-dioxopyrrol-1-yl)decyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names N,N'-Decamethylendimaleinimid

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:39763-02-5 SDS

39763-02-5Downstream Products

39763-02-5Relevant articles and documents

An efficient reverse Diels-Alder approach for the synthesis of N-alkyl bismaleimides

Rao, Venkataramanarao,Navath, Suryakiran,Kottur, Mohankumar,McElhanon, James R.,McGrath, Dominic V.

, p. 5011 - 5013 (2013/09/02)

Bismaleimides are useful precursors for Diels-Alder reactions, Michael additions, and thiol-maleimide based conjugation for the synthesis of materials and polymers. Use of bismaleimide cross linkers for generating polymers, bioconjugate molecules, and useful imaging molecules is an active area of research. An efficient and practical synthetic protocol for N-alkyl bis-maleimide cross linkers starting from furan protected maleimide employing a reverse Diels-Alder reaction is reported.

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