33831-38-8

Basic information

• Product Name: 2-bromo-2-phenyladamantane
• Synonyms: 2-bromo-2-phenyladamantane
• CAS NO: 33831-38-8
• Molecular Weight: 291.231
• Mol File: 33831-38-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-bromo-2-phenyladamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-2-phenyladamantane(33831-38-8)
• EPA Substance Registry System: 2-bromo-2-phenyladamantane(33831-38-8)

Safety Data

• Hazardous Substances Data: 33831-38-8(Hazardous Substances Data)

Upstream product

• 700-58-3 2-Adamantanone 
• 281-23-2 adamantane 
• 19066-24-1 2-Phenyladamantane 
• 29480-18-0 2-phenyladamantan-2-ol 

Downstream Products

• 51940-11-5 2,4,6-triphenylverdazylium bromide 
• 87840-08-2 3-Adamantyliden-6-(2-phenyl-2-adamantyl)-1,4-cyclohexydien 
• 129302-84-7 2-phenyladamantane-2-d 

Relevant articles and documents

Kinetics and mechanism of unimolecular heterolysis of carcass compounds. XV. The nature of solvation effects in heterolysis of 2-bromo-2-phenyladamantane in dipolar aprotic solvents

Heterolysis kinetics of 2-bromo-2-phenyladamantane in MeCN,γ-butyrolactone, sulfolane, and cyclohexanone were studied with verdazyl method. The rate is described by an equation w = k[RBr], and the reaction proceeds by SN1 mechanism. The decreas

Thermolabile Hydrocarbons, XX. Synthesis, Structure, and Strain of Sym. Tetraalkyl-1,2-diarylethanes

The syntheses of 18 1,1,2,2-tetraalkyl-1,2-diarylethanes 1 - 4 by dimerisation procedures starting with 10 - 13 are reported.In the absence of p-substituents X and with increasing alkyl side chains the α,p-dimers 6 or their aromatic counter parts 7 are obtained besides or instead of 1.The relationships between strain enthalpy Hs, bond lengths, bond angles, torsional angles, and rotational barrier are discussed on the basis of force field calculations.They are supported by two additional experimental structure determinations by X-ray diffraction.