1229227-01-3

Basic information

• Product Name: C₁₈H₁₂B₃Br₃O₃
• Synonyms: C₁₈H₁₂B₃Br₃O₃
• CAS NO: 1229227-01-3
• Molecular Weight: 548.436
• Mol File: 1229227-01-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₂B₃Br₃O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₂B₃Br₃O₃(1229227-01-3)
• EPA Substance Registry System: C₁₈H₁₂B₃Br₃O₃(1229227-01-3)

Safety Data

• Hazardous Substances Data: 1229227-01-3(Hazardous Substances Data)

Upstream product

• 244205-40-1 (2-bromophenyl)boronic acid 

Downstream Products

• 87698-82-6 4-(2-bromophenyl)morpholine 
• 1075193-04-2 N,N-dibenzyl-2-bromoaniline 
• 40138-16-7 2-formylbenzene boronic acid 
• 149105-19-1 2-carboxyphenylboronic acid 
• 1229227-08-0 C₁₅H₁₄BrNO 

Relevant articles and documents

A process for preparing aldehyde group benzene boric acid

The invention discloses a method for preparing formyl phenylboronic acid, which comprises the following steps: heating halogenated phenylboronic acid in toluene or heptane under reflux for dewatering to form a tripolymer, mixing the tripolymer with dimethylformamide, dropwisely adding n-butyllithium at low temperature to react by a one-pot process, hydrolyzing with hydrochloric acid, and recrystallizing to obtain the formyl phenylboronic acid. The method is simple to operate, avoids the process of separating the intermediate after formyl protection in the conventional technique, has high universality, can obtain favorable yield for ortho-, meta- and para- formyl phenylboronic acids, and is beneficial to scale-up production.

Transition-metal-free electrophilic amination of arylboroxines

A transition-metal-free strategy to construct C(sp2)-N bonds using arylboroxines and O-benzoyl hydroxylamines as coupling partners has been developed. This transformation provides a useful method to access various aromatic amines.