27575-78-6

Basic information

• Product Name: 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene
• Synonyms: 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene;c(ccc(c1)Cl)(c1)C(c(ccc(c2)Cl)c2)c(ccc(c3)Cl)c3
• CAS NO: 27575-78-6
• Molecular Formula: C₁₉H₁₃Cl₃
• Molecular Weight: 347.67
• Mol File: 27575-78-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 441.6°Cat760mmHg
• Flash Point: 312.2°C
• Appearance: /
• Density: 1.294g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene(27575-78-6)
• EPA Substance Registry System: 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene(27575-78-6)

Safety Data

• Hazardous Substances Data: 27575-78-6(Hazardous Substances Data)

Usage

Uses

Tris(4-chlorophenyl)methane is a standard for environmental testing and research. Studies on the geographical distribution, accumulation kinetics and infants health risk of organochlorines in human breast milk from Indonesia. Extraction and cleanup methods for analysis of phenolic and neutral organohalogens in plasma.

Upstream product

• 34875-71-3 bis(4-chlorophenyl)methyl diethyl phosphate 
• 108-90-7 chlorobenzene 
• 90-97-1 4,4'-dichlorobenzophenone 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 5418-23-5 tetrakis-(4-chloro-phenyl)-ethane-1,2-diol 
• 789-02-6 o,p'-DDT 
• 50-29-3 p,p'-DDT 
• 75-87-6 chloral 
• 3010-80-8 tris(p-chlorophenyl)methanol 
• 19920-03-7 1,2,2,2-tetrakis-(p-chlorophenyl)ethanone 

Downstream Products

• 3010-80-8 tris(p-chlorophenyl)methanol 
• 90-98-2 4,4'-Dichlorobenzophenone 

Relevant articles and documents

Benzylic Phosphates in Friedel-Crafts Reactions with Activated and Unactivated Arenes: Access to Polyarylated Alkanes

Easily reachable electron-poor/rich primary and secondary benzylic phosphates are suitably used as substrates for Friedel-Crafts benzylation reactions with only 1.2 equiv activated/deactivated arenes (no additional solvent) to access structurally and electronically diverse polyarylated alkanes with excellent yields and selectivities at room temperature. Specifically, diversely substituted di/triarylmethanes are generated within 2-30 min using this approach. A wide number of electron-poor polyarylated alkanes are easily accomplished through this route by just tuning the phosphates.

DDT, a potentiaal source of environmental tris(4-chlorophenyl)methane and tris(4-chlorophenyl) methanol

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