N-(2,4,6-Tribromophenyl)maleimide CAS 59789-51-4

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
• Links
• Quick Inquiry

Iden­ti­fi­ca­tion

CAS Number

59789-51-4

Name

N-(2,4,6-Tribromophenyl)maleimide

Syn­onyms

1-(2,4,6-tribromophenyl)pyrrole-2,5-dione

SMILES

C1=CC(=O)N(C1=O)C2=C(C=C(C=C2Br)Br)Br

Std­InChI

InChI=1S/C10H4Br3NO2/c11-5-3-6(12)10(7(13)4-5)14-8(15)1-2-9(14)16/h1-4H

Std­InChIKey

ONEIBT­GSNPDDSB-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C10H4Br3NO2

Mol­e­c­u­lar Weight

409.86

Prop­er­ties

Appear­ance

Light yel­low powder

Safe­ty Data

RIDADR 

NONH for all modes of transport

WGK Germany

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our N-(2,4,6-Tribromophenyl)maleimide CAS 59789-51-4

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Assay

97%min

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

Can be used in aero­space com­pos­ite mate­ri­als (high tem­per­a­ture heat resis­tance); PCB elec­tron­ic insu­la­tion mate­ri­als (good flame retar­dan­cy); 3D print­ing pho­to­sen­si­tive resins (high reac­tiv­i­ty); high-per­­for­­mance coat­ings, adhe­sives (reac­tive structures)

1. High-per­­for­­mance poly­mer addi­tives or monomers
   Used to syn­the­size spe­cial ther­moset­ting resins or high-tem­per­a­­ture resis­tant poly­mers, such as poly­imide and maleimide copoly­mers ; its maleimide struc­ture can under­go addi­tion poly­mer­iza­tion, free rad­i­cal poly­mer­iza­tion or Diels-Alder reac­tion with oth­er monomers ; the aro­mat­ic tri­bro­mo sub­sti­tu­tion group gives the prod­uct flame retar­dan­cy and ther­mal sta­bil­i­ty, suit­able for use in high-per­­for­­mance mate­ri­als such as avi­a­tion, elec­tron­ics, and insulation.
2. Flame retar­dant inter­me­di­ates or syn­er­gists
   The Br (bromine) ele­ment on the aro­mat­ic ring has excel­lent flame retar­dant effect ; this prod­uct can be used as a reac­tive flame retar­dant inter­me­di­ate, embed­ded in the main chain or side chain of the poly­mer to improve the flame retar­dant effi­cien­cy and reduce migra­tion ; it is often used for effi­cient flame retar­dant mod­i­fi­ca­tion of poly­ester, polyamide, epoxy resin and oth­er systems.
3. Elec­tron­ic mate­r­i­al inter­me­di­ates
   N-aryl maleimide com­pounds have excel­lent elec­tron­ic prop­er­ties and are wide­ly used in : organ­ic semi­con­duc­tors, opto­elec­tron­ic func­tion­al mate­ri­als, pho­tore­sists and oth­er func­tion­al poly­mer monomers. After tri­bro­mo sub­sti­tu­tion, it can be fur­ther deriva­tized, such as par­tic­i­pat­ing in Suzu­ki or Stille cou­pling to con­struct a π con­ju­gat­ed system.
4. Photosensitizer/​crosslinker
   Maleimide groups have good elec­tron affin­i­ty and are often used in pho­­to-ini­ti­at­ed crosslink­ing reac­tions or UV cur­ing sys­tems. They can be rapid­ly pho­tocrosslinked with thi­ols and alkenes to form a crosslinked net­work struc­ture, which is used in pho­tore­sists, adhe­sives and oth­er fields.

Prod­uct features

High ther­mal sta­bil­i­ty ; Excel­lent flame retar­dant prop­er­ties ; Easy to mod­i­fy ; High photo/​thermal reac­tiv­i­ty ; Good compatibility

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Warshel Chem­i­cal Ltd (https://​www​.warshel​.com/).

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