57263-21-5

Basic information

• Product Name: Benzene, 1-bromo-4-(1,1-dimethylpropyl)-
• CAS NO: 57263-21-5
• Molecular Formula: C11H15Br
• Molecular Weight: 227.144
• Mol File: 57263-21-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-4-(1,1-dimethylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-4-(1,1-dimethylpropyl)-(57263-21-5)
• EPA Substance Registry System: Benzene, 1-bromo-4-(1,1-dimethylpropyl)-(57263-21-5)

Safety Data

• Hazardous Substances Data: 57263-21-5(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 107-84-6 1-chloro-3-methylbutane 
• 80-46-6 4-t-amylphenol 
• 851231-25-9 [4-(1,1-dimethylpropyl)phenyl]trifluoromethanesulfonate 
• 851199-04-7 2-[4-(1,1-dimethylpropyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 2049-95-8 tery-amylbenzene 

Downstream Products

• 57263-20-4 1-[4-(1,1-dimethyl-propyl)-phenyl]-2,2,4,4-tetramethyl-3-(4-pyridin-2-yl-piperazin-1-yl)-cyclobutanol 
• 586-76-5 4-Bromobenzoic acid 

Relevant articles and documents

Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940

A series of 1-deoxy analogs of CP-47,497 (8 and 13, n = 0-7) and 1-deoxy analogs of CP-55,940 (9, n = 0-7) have been synthesized and their affinities for the cannabinoid CB1 and CB2 receptors have been determined. Although the majori

The Synthesis of Bridged Oligophenylenes from Fluorene 1. Terphenyls and Quaterphenyls

Improved methods are presented for the alkylation of fluorene (2) to 9,9- dialkylfluorenes (3-6) free from 9-monoalkylfluorenes.Mono- and dihalogenated derivatives of 2-6 are reported as are a variety of ring substituted 9,9-dialkylfluorenes.Halogenated 9,9-dialkylfluorenes and aryl or methyl Grignard reagents were cross-coupled in Pd-catalyzed reactions to generate a series of novel p-oligophenylenes (four terphenyls (26, 27, 29 and 31c) and nineteen quterphenyls (33-6, 64-71 and 73-79)) each possessing one or two dialkylated methylene bridges between aromatic rings.Each bridged oligophneylene showed enhanced solubility, high quantum efficiency and photochemical stability.A number of quaterphenyls incorporated substituents which extended the conjugation of the oligophenylene chromophore.