N-(2,4,6-Trichlorophenyl)maleimide CAS 13167-25-4

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

Iden­ti­fi­ca­tion

CAS Number

13167-25-4

Name

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

Syn­onyms

1-(2,4,6-Trichlorophenyl)-1H-pyrrole-2,5-dione

SMILES

C1=CC(=O)N(C1=O)C2=C(C=C(C=C2Cl)Cl)Cl

Std­InChI

InChI=1S/C10H4Cl3NO2/c11-5-3-6(12)10(7(13)4-5)14-8(15)1-2-9(14)16/h1-4H

Std­InChIKey

VHZJ­­MA­JCUAW­I­HV-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C10H4Cl3NO2

Mol­e­c­u­lar Weight

276.5

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-Trichlorophenyl)maleimide CAS 13167-25-4

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Assay

97%min

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

1. High-per­­for­­mance poly­mer inter­me­di­ates
   This com­pound is often used to pre­pare heat-resis­­tant and insu­lat­ing poly­mers, such as poly­imide and maleimide copoly­mers ; it can be used as a comonomer of ther­moset­ting resins to give the mate­r­i­al high strength and ther­mal oxy­gen sta­bil­i­ty ; chlo­rine atoms enhance the flame retar­dan­cy and chem­i­cal cor­ro­sion resis­tance of the mate­r­i­al.
   Used in aero­space com­pos­ites ; high-end electronic/​electrical insu­la­tion mate­ri­als ; high-tem­per­a­­ture adhe­sives or coatings.
2. Pho­to­sen­si­tive mate­ri­als and crosslink­ers
   The maleimide struc­ture makes it suit­able for UV cur­ing and ther­mal crosslink­ing sys­tems ; the struc­ture has high rigid­i­ty and is often used as a monomer for pho­tore­sists, liq­uid crys­tal ori­ent­ing agents or pho­to­sen­si­tive poly­mers ; it can be used in con­junc­tion with pho­toini­tia­tors for elec­tron­ic pack­ag­ing materials.
3. Phar­ma­ceu­ti­cal or pes­ti­cide inter­me­di­ates (poten­tial)
   Chloroaryl groups have cer­tain antibac­te­r­i­al, anti­fun­gal or insec­ti­ci­dal prop­er­ties, and can the­o­ret­i­cal­ly be used as pre­cur­sors for cer­tain pes­ti­cide or phar­ma­ceu­ti­cal active mol­e­cules ; maleimide groups are often used to syn­the­size het­e­ro­cyclic drug can­di­dates with diverse struc­tures (such as the par­ent nucle­us of anti­cancer and antivi­ral drugs);
4. Spe­cial addi­tives or func­tion­al coat­ing mate­ri­als
   Trichloro­sub­sti­tut­ed groups make them hydropho­bic and antimi­cro­bial ; they can be used to syn­the­size antibac­te­r­i­al poly­mer coat­ings, func­tion­al­ize the sur­face of med­ical devices, and mod­i­fy mem­brane mate­ri­als ; they are suit­able for coat­ing sys­tems with sol­vent resis­tance, scratch resis­tance, and anti-aging functions.

Prod­uct features

High ther­mal sta­bil­i­ty ; Strong elec­tron affin­i­ty ; Flame retar­dant ; Good chem­i­cal resis­tance ; Adjustable functions

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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