1020180-02-2

Basic information

• Product Name: 3-bromo-N-(diphenylmethylene)-benzenamine
• Synonyms: 3-bromo-N-(diphenylmethylene)-benzenamine
• CAS NO: 1020180-02-2
• Molecular Weight: 336.231
• Mol File: 1020180-02-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-bromo-N-(diphenylmethylene)-benzenamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-N-(diphenylmethylene)-benzenamine(1020180-02-2)
• EPA Substance Registry System: 3-bromo-N-(diphenylmethylene)-benzenamine(1020180-02-2)

Safety Data

• Hazardous Substances Data: 1020180-02-2(Hazardous Substances Data)

Upstream product

• 119-61-9 benzophenone 
• 591-19-5 m-Bromoaniline 
• 1013-88-3 Benzophenone imine 
• 108-36-1 1,3-dibromobenzene 

Downstream Products

• 210907-84-9 3-aminophenylboronic acid pinacolate 
• 1257310-88-5 [3-(benzhydrylideneamino)phenyl]carbamic acid 2-trimethylsilanylethyl ester 
• 30418-59-8 3-Aminophenylboronic acid 

Relevant articles and documents

Process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters

The present invention relates to a process for the preparation of aminoaryl- and aminoheteroaryl boronic acids and esters of formula (I) in high yields The claimed process uses diarylketal formula (V) to generate an arylbromid of formula (III) in which the amino-group is protected as bisarylmethylidenimino-group:

Preparation of Aminoaryl and Aminoheteroaryl Boronic Acids and Derivatives Thereof

The invention relates to a method for preparation of aminoaryl- or aminoheteroarylboronic acids and esters and salts thereof in which an optionally substituted aminoaryl or aminoheteroaryl compound is protected at its nitrogen site via condensation with a carbonyl compound, subsequently metalated and converted with a suitable boron compound. Depending on the subsequent work-up and removal of the protective group, the corresponding boronic acid, the anhydride or the boronic acid ester thereof is obtained