CAS 698-00-0
:2-Bromo-N,N-dimetilbenzenammina
- (2-Bromophenyl)dimethylamine
- 1-Bromo-2-dimethylaminobenzene
- 2-(Dimethylamino)bromobenzene
- 2-(Dimethylamino)phenyl bromide
- 2-(N,N-Dimethylamino)bromobenzene
- 2-Dimethylamino-1-bromobenzene
- 2-bromo-N,N-dimethylbenzenamine
- Aniline, o-bromo-N,N-dimethyl-
- N,N-Dimethyl-2-bromoaniline
- NSC 33816
- benzenamine, 2-bromo-N,N-dimethyl-
- o-Bromo-N,N-dimethylaniline
- Vedi altri sinonimi
2-Bromo-N,N-dimethylaniline
CAS:Formula:C8H10BrNPurezza:>98.0%(GC)(T)Colore e forma:Colorless to Light orange to Yellow clear liquidPeso molecolare:200.082-Bromo-N,N-dimethylaniline, min. 98%
CAS:Formula:C8H10BrNPurezza:min. 98%Colore e forma:colorless to pale yellow liquidPeso molecolare:200.082-Bromo-N,N-dimethylaniline
CAS:Formula:C8H10BrNPurezza:95%Colore e forma:LiquidPeso molecolare:200.0792-Bromo-N,N-dimethylaniline
CAS:2-Bromo-N,N-dimethylaniline is a chemical compound that belongs to the class of alkylating agents. It is prepared by the reaction of 2-bromoaniline with a Grignard reagent, followed by acidification and removal of the volatile bromide. 2-Bromo-N,N-dimethylaniline has been used in the preparation of ligands for metal complexes and as an acetal protecting group for alcohols and phenols. 2-Bromo-N,N-dimethylaniline has been shown to be a good cross-coupling agent for halides or aromatic heterocycles, which is an important property in organic synthesis. The mechanism involves initial abstraction of hydrogen from the substrate molecule by 2-bromo-N,N-dimethylaniline forming an intermediate cationic species. This intermediate cationic species then reacts with the substrate molecule
Formula:C8H10BrNPurezza:Min. 95%Peso molecolare:200.08 g/mol2-Bromo-N,N-dimethylaniline
CAS:Formula:C8H10BrNPurezza:98.0 min. %Colore e forma:colorless to pale yellow liquidPeso molecolare:200.08





