2810-69-7

Basic information

• Product Name: 3,4,5,6-TETRABROMO-O-XYLENE
• Synonyms: 3,4,5,6-TETRABROMO-O-XYLENE;1,2-Dimethyltetrabromobenzene;o-Xylene, 3,4,5,6-tetrabromo-;Tetrabromo-ortho-xylene;Tetrabromo-o-xylene;Benzene, 1,2,3,4-tetrabromo-5,6-dimethyl-
• CAS NO: 2810-69-7
• Molecular Formula: C₈H₆Br₄
• Molecular Weight: 421.75
• Mol File: 2810-69-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 262°C
• Boiling Point: 303.01°C (rough estimate)
• Flash Point: 177.6°C
• Appearance: /
• Density: 2.2654 (rough estimate)
• Refractive Index: 1.7040 (estimate)
• CAS DataBase Reference: 3,4,5,6-TETRABROMO-O-XYLENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5,6-TETRABROMO-O-XYLENE(2810-69-7)
• EPA Substance Registry System: 3,4,5,6-TETRABROMO-O-XYLENE(2810-69-7)

Safety Data

• Hazardous Substances Data: 2810-69-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H6Br4/c1-3-4(2)6(10)8(12)7(11)5(3)9/h1-2H3

Upstream product

• 4132-77-8 3,4-dimethylcumene 
• 95-47-6 o-xylene 
• 7726-95-6 bromine 
• 7553-56-2 iodine 
• 7790-94-5 chlorosulfonic acid 
• 62133-11-3 4-(1-Adamantyl)-1,2-dimethylbenzene 

Downstream Products

• 13810-83-8 tetrabromobenzene-1,2-dicarboxylic acid 
• 1206837-88-8 1,2,3,4-tetra(4'-t-butylphenylthio)-5,6-dimethylbenzene 
• 1402159-54-9 C₄₁H₃₇NO₅ 
• 1402159-58-3 C₈H₄Br₄ 
• 31619-41-7 2-methoxy-1,4-anthracenedione 
• 114861-42-6 4,5,6,7-Tetrabrom-2-(p-tolylsulfonyl)-2,3-dihydro-1H-isoindol 
• 168787-63-1 1,2,3,4-Tetrakis-(1-chloro-3,3-diphenyl-propa-1,2-dienyl)-5,6-dimethyl-benzene 
• 932745-92-1 diethyl 2-(benzyloxycarbonylamino)-4,5,6,7-tetrabromoindane-2-phosphonate 
• 168787-62-0 Tetrakis(3-hydroxy-3,3-diphenyl-1-propinyl)-o-xylol 
• 53042-28-7 1,2-bis(bromomethyl)-3,4,5,6-tetrabromobenzene 
• 1206837-90-2 5,6,7,8-tetra(4'-t-butylphenylthio)anthracene-1,4-dione 
• 1206837-89-9 1,2,3,4-tetra(4'-t-butylphenylthio)-5,6-bis(bromomethyl)benzene 

Relevant articles and documents

Diversity oriented approach to polycyclic compounds through the diels-alder reaction and the Suzuki coupling

A diversity oriented strategy has been demonstrated to deliver small "drug like" molecules using alkylation, Diels-Alder reaction, and Suzuki-Miyaura cross-coupling as key steps. This methodology allows access a wide range of molecules using simple scaffolds such as indanes, tetralins and tetrahydroisoquinolines, which can enhance the chemical space for potential therapeutic molecules.

Design, synthesis, and characterization of a persistent nonacene derivative

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SYNTHESIS OF 3-(ALKYLARYL)-1-ADAMANTANOLS

The possibility was demonstrated for removal of hydride ions from 1-(alkylaryl)adamantanes by tertiary carbocations generated from the corresponding alcohols or halides in trifluoroacetic acid leading to the formation of 3-(alkylaryl)-1-adamantanols in 40-60percent yield.In the case of 1-phenyladamantane, the major product is 1-(1-adamantyl)-4-benzene formed in 71percent yield due to presence of two reaction sites (the benzene ring para position and the tertiary carbon atom of the adamantane fragment) in the starting 1-phenyladamantane.