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Name: 1,3,5-Tris(bromomethyl)benzene   

CAS NO: 18226-42-1

MF: C9H9Br3

MW: 356.88

MP: 94-99?C

BP:352.2±37.0 °C at 760 mmHg

Density:2.0±0.1 g/cm3

Appearance: white solid

Purity: 97% min

Package: 25g, 100g, 500g, bulk package 

Application:OLED intermediate

Tris(bromomethyl)benzene is an isomeric mixture of 1,3,5-tris(bromomethyl)benzene CAS NO: 18226-42-1 and 1,3-bis(bromomethyl)benzene. It is used in the synthesis of various organic compounds such as acylation reactions, which are reactions that use an acid to introduce an acyl group into a molecule. The reaction products can be monoclonal antibodies or drug substances. The terminal half-life for Tris(bromomethyl)benzene ranges from 2 to 3 hours. It has been shown to be reactive and cavity-forming, with reactive properties that allow it to form adducts with nucleophiles such as serine protease or hydrochloric acid. Tris(bromomethyl)benzene also has been used in the Suzuki coupling reaction with tetrahydrofuran and phenethyl boronic

Other name:

α,α',α''-罢谤颈产谤辞尘辞尘别蝉颈迟测濒别苍别;

Benzene, 1,3,5-tris(bromomethyl)-;

tris-(Bromomethyl)benzene;

1,3,5-Tris(bromomethyl)benzene CAS NO: 18226-42-1 has three bromo substituents around an aromatic ring that can be used as a cross-linker. It is mainly utilized in the synthesis of ligands and dendrimeric monomers.

Tris(bromomethyl)benzene is an isomeric mixture of 1,3,5-tris(bromomethyl)benzene  CAS NO: 18226-42-1  and 1,3-bis(bromomethyl)benzene.

 It is used in the synthesis of various organic compounds such as acylation reactions, which are reactions that use an acid to introduce an acyl group into a molecule. 

The reaction products can be monoclonal antibodies or drug substances. The terminal half-life for Tris(bromomethyl)benzene ranges from 2 to 3 hours. 

It has been shown to be reactive and cavity-forming, with reactive properties that allow it to form adducts with nucleophiles such as serine protease or hydrochloric acid. Tris(bromomethyl)benzene also has been used in the Suzuki coupling reaction with tetrahydrofuran and phenethyl boronic.

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