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α-Bromostyrene cation is a chemical species derived from the protonation of α-bromostyrene, a halogenated aromatic compound. It consists of a benzene ring with a bromine atom attached to the carbon atom adjacent to the double bond, and a positively charged carbon atom at the α-position (next to the bromine). This cation is generated when α-bromostyrene loses a hydrogen atom, typically in the presence of a strong acid. The α-bromostyrene cation is an important intermediate in various organic reactions, such as electrophilic aromatic substitution and the formation of Grignard reagents. Its stability is attributed to the resonance delocalization of the positive charge across the benzene ring and the inductive effect of the bromine atom, which withdraws electron density from the cationic center.

84648-98-6

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84648-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84648-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84648-98:
(7*8)+(6*4)+(5*6)+(4*4)+(3*8)+(2*9)+(1*8)=176
176 % 10 = 6
So 84648-98-6 is a valid CAS Registry Number.

84648-98-6Upstream product

84648-98-6Downstream Products

84648-98-6Relevant academic research and scientific papers

Absorption Spectra and Photochemical Rearrangements of Alkyl- and Dialkylbenzene Cations in Solid Argon

Kelsall, Benuel J.,Andrews, Lester

, p. 5893 - 5898 (2007/10/02)

Matrix photoionization of alkyl- and dialkylbenzenes produced and trapped the parent radical cations.Irradiation in the visible parent cation absorption induced α-H transfer to the cation ring to give substituted methylenecyclohexadiene cations.The ease of 1,3-hydrogen transfer in these experiments suggests that this may be an important rearrangement in gaseous alkylbenzene cations.Subsequent ultraviolet photolysis of these samples produced substituted styrene cations.

Absorption Spectra and Photochemical Rearrangements of Chlorostyrene and Bromostyrene Cations in Solid Argon at 20 K

Kelsall, Benuel J.,Andrews, Lester,Schwarz, Helmut

, p. 1295 - 1300 (2007/10/02)

Matrix photoionization experiments with chloro- and bromostyrenes at high dilution in argon have produced and trapped the parent cations as identified by strong absorptions in the red and near-UV regions.Photolysis rearranged the α isomers to the Z and E β isomers with a larger yield of the E β isomer.The Z- and E-β isomers were interconverted by selective photoexcitation.Photolysis of α-bromostyrene cation also produced the phenylacetylene cation.

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