635305-38-3

Basic information

• Product Name: 1,3,2-Dioxaborinane, 2-(3-bromophenyl)-5,5-dimethyl-
• CAS NO: 635305-38-3
• Molecular Formula: C11H14BBrO2
• Molecular Weight: 268.946
• Mol File: 635305-38-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,3,2-Dioxaborinane, 2-(3-bromophenyl)-5,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,2-Dioxaborinane, 2-(3-bromophenyl)-5,5-dimethyl-(635305-38-3)
• EPA Substance Registry System: 1,3,2-Dioxaborinane, 2-(3-bromophenyl)-5,5-dimethyl-(635305-38-3)

Safety Data

• Hazardous Substances Data: 635305-38-3(Hazardous Substances Data)

Usage

Type of compound

Boronic acid derivative

Usage

Building block for pharmaceuticals and agrochemicals

Structural features

Boron-containing ring structure
Bromine-substituted phenyl group
Two methyl groups

Reactions

Suzuki-Miyaura cross-coupling reactions
Formation of carbon-carbon bonds

Potential applications

Fluorescent probe for detecting specific biomolecules in biological systems

Upstream product

• 89598-96-9 (3-bromophenyl)boronic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 

Downstream Products

• 1453098-84-4 (3-bromophenyl)(2-(pyridin-2-yl)phenyl)methanone 
• 16400-51-4 3,3'-dibromobiphenyl 
• 88-72-2 1-methyl-2-nitrobenzene 
• 552-89-6 2-nitro-benzaldehyde 
• 884010-26-8 2,2-dimethylpropane-1,3-diyl [3-trimethylsilylethynylphenyl] boronate 
• 866270-03-3 2-(3-bromophenyl)-N-methoxy-N-methylacetamide 
• 951884-73-4 2-(3-bromophenyl)-1-(pyrrolidin-1-yl)ethanone 
• 14062-30-7 ethyl 2-(3-bromophenyl)acetate 
• 56911-48-9 diethyl (3-bromophenyl)malonate 

Relevant articles and documents

Ruthenium-Catalyzed Carbonylative Coupling of Anilines with Organoboranes by the Cleavage of Neutral Aryl C-N Bond

Herein, we report the first ruthenium-catalyzed Suzuki-type carbonylative reaction of electronically neutral anilines via C(aryl)-N bond cleavage. Without any ligand and base, diaryl ketones can be obtained in moderate to high yields by using Ru3/su

Selective Monoarylation of Aromatic Ketones and Esters via Cleavage of Aromatic Carbon-Heteroatom Bonds by Trialkylphosphine Ruthenium Catalysts

We report here the ruthenium-catalyzed selective monoarylation of aromatic ketones bearing two ortho carbon-heteroatom (O or N) bonds. Under the newly developed catalyst system consisting of RuHCl(CO)(PiPr3)2, CsF, and sty

PHARMACEUTICAL USE OF BORONIC ACIDS AND ESTERS THEREOF

Use of compounds to inhibit hormone-sensitive lipase, the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, method of treatment employing these compounds and compositions, and novel compounds. The present compounds are inhibitors of hormone-sensitve lipase and may be useful in the treatment and/or prevention of a range of medical disorders where a decreased activity of hormone-sensitive lipase is desirable.