2,3-Dibromobenzotrifluoride is an aromatic compound characterized by the presence of bromine and trifluoromethyl groups attached to a benzene ring. Its molecular structure features two bromine atoms located at the 2 and 3 positions of the benzene ring, along with three fluorine atoms at the 1, 1', and 1'' positions, contributing to its unique reactivity and properties. This compound is typically a colorless to pale yellow liquid with a relatively high density and low volatility. It is known for its stability under normal conditions but can undergo reactions typical of aromatic halides, such as nucleophilic substitution. The presence of both bromine and trifluoromethyl groups enhances its electron-withdrawing characteristics, making it useful in various chemical applications, including as an intermediate in organic synthesis and in the production of specialty chemicals. Safety precautions should be taken when handling this compound, as it may pose health risks due to its halogenated nature.

2,3-Dibromobenzotrifluoride

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1,2-Dibromo-3-(trifluoromethyl)benzene

1,2-Dibromo-3-(trifluoromethyl)benzene (1,2-DBTFB) is a reactive brominating agent that can be used to attack C=C bonds. It has a high selectivity for the C=C bond as opposed to other bonds in the molecule. 1,2-DBTFB reacts with lithium metal or an alkyllithium to form a metalated product. The regioselectivity of this reaction is controlled by the position of substitution on the benzene ring. 1,2-DBTFB can be used to isomerize substituents at positions adjacent to the bromine atom and deprotonate halogens.

CAS 493038-92-9: 2,3-Dibromobenzotrifluoride

1,2-Dibromo-3-(trifluoromethyl)benzene

Ref: 10-F319269

2,3-Dibromobenzotrifluoride

Ref: 54-PC0323

1,2-Dibromo-3-(trifluoromethyl)benzene

Ref: 3D-FD84527

2,3-DIBROMOBENZOTRIFLUORIDE

Ref: IN-DA00DTHU