40860-87-5

Basic information

• Product Name: α,α,α',α',α'',α'',2,4,6-nonachloromesitylene
• Synonyms: α,α,α',α',α'',α'',2,4,6-nonachloromesitylene
• CAS NO: 40860-87-5
• Molecular Weight: 430.2
• Mol File: 40860-87-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: α,α,α',α',α'',α'',2,4,6-nonachloromesitylene(CAS DataBase Reference)
• NIST Chemistry Reference: α,α,α',α',α'',α'',2,4,6-nonachloromesitylene(40860-87-5)
• EPA Substance Registry System: α,α,α',α',α'',α'',2,4,6-nonachloromesitylene(40860-87-5)

Safety Data

• Hazardous Substances Data: 40860-87-5(Hazardous Substances Data)

Upstream product

• 108-67-8 1,3,5-trimethyl-benzene 
• 108-70-3 1,3,5-trichlorobenzene 
• 67-66-3 chloroform 
• 5324-68-5 1,3,5-trichloro-2,4,6-trimethylbenzene 

Downstream Products

• 144811-66-5 2,4,6-trichloro-α,α,α',α',α'',α''-hexakis(pentachlorophenyl)mesitylene 
• 14725-92-9 2.4.6-Trichlor-benzoltrialdehyd-(1.3.5)-trioxim 
• 2243590-42-1 benzo[1,2-b:3,4-b':5,6-b]trithiophene-2,5,8 tricarbaldehyde 
• 14222-98-1 2,4,6-trichlorobenzene-1,3,5-tricarbaldehyde 

Relevant articles and documents

Benzotrithiophene-Based Covalent Organic Frameworks: Construction and Structure Transformation under Ionothermal Condition

A C3-symmetric benzotrithiophene tricarbaldehyde (BTT) is synthesized for the first time with a facile method, which is used to construct BTT-based covalent organic frameworks (COFs) with different pore sizes. Meanwhile, the structure transform

π-Conjugated Microporous Polymer Films: Designed Synthesis, Conducting Properties, and Photoenergy Conversions

Conjugated microporous polymers are a unique class of polymers that combine extended π-conjugation with inherent porosity. However, these polymers are synthesized through solution-phase reactions to yield insoluble and unprocessable solids, which preclude

Stable polyradicals with high-spin ground states. 2. synthesis and characterization of a complete series of polyradicals derived from 2,4,6-trichloro-α,α,α′,α′,α″, α″-hexakis(pentachlorophenyl)mesitylene with S = 1/2, 1, and 3/2 ground states1,2

The series of stable polyradicals 2-4 was synthesized via the title mesitylene hydrocarbon. Cyclic voltammetry of radicals 2-4 revealed, in accordance with the number of radical centers and their topologies, several reversible one-electron reduction proce