183677-71-6

Basic information

• Product Name: 4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER
• Synonyms: AKOS BRN-1100;4-BROMOPHENYLBORONIC ACID NEOPENTYL GLYCOL CYCLIC ESTER;4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL CYCLIC ESTER;4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER;2-(4-Bromophenyl)-5,5-dimethyl-1,3,2-dioxaborinane;4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER, 98+%;4-Bromophenylboronic acidneopentylglycol ester
• CAS NO: 183677-71-6
• Molecular Formula: C₁₁H₁₄BBrO₂
• Molecular Weight: 268.94
• EINECS: -0
• Product Categories: Boronic acids
• Mol File: 183677-71-6.mol
• Article Data: 20

Chemical Properties

• Melting Point: 109-111°C
• Boiling Point: 331°Cat760mmHg
• Flash Point: 154°C
• Appearance: /
• Density: 1.33g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.533
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER(183677-71-6)
• EPA Substance Registry System: 4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER(183677-71-6)

Safety Data

• Safety Statements: 22-24/25
• Hazardous Substances Data: 183677-71-6(Hazardous Substances Data)

Usage

General Description

4-Bromobenzeneboronic acid neopentyl glycol ester is a chemical compound used in organic synthesis and medicinal chemistry research. It is a boronic acid derivative that contains a neopentyl glycol ester group, making it a versatile building block for the synthesis of various organic molecules. 4-BROMOBENZENEBORONIC ACID NEOPENTYL GLYCOL ESTER has been utilized in the development of pharmaceuticals and agrochemicals, as well as in the production of materials such as liquid crystals and polymers. The neopentyl glycol ester moiety provides stability and protection for the boronic acid functionality, allowing for the efficient and controlled manipulation of the compound in chemical reactions. Overall, 4-bromobenzeneboronic acid neopentyl glycol ester is a valuable tool for the design and synthesis of biologically active compounds and functional materials.

InChI:InChI=1/C11H14BBrO2/c1-11(2)7-14-12(15-8-11)9-3-5-10(13)6-4-9/h3-6H,7-8H2,1-2H3

Upstream product

• 941-98-0 1'-naphthacetophenone 
• 5467-74-3 4-Bromophenylboronic acid 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 17946-45-1 tris-(4-bromophenyl)stibine 
• 201733-56-4 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 183677-72-7 2,2-dimethylpropane-1,3-diyl [4-(trimethylsilylethynyl)phenyl] boronate 
• 630127-51-4 4-[(trimethylsilyl)ethynyl]phenyl boronic acid 
• 106-38-7 para-bromotoluene 
• 63996-36-1 2-(4-bromophenyl]pyridine 
• 1244016-74-7 4-(aldehydephenylethynyl)benzene boronic acid neopentyl glycol ester 
• 1467060-40-7 3-[4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)phenoxy]-2,2-dimethylpropan-1-ol 
• 1467060-32-7 5,5-dimethyl-2-[4-(oxetan-3-yloxy)phenyl]-1,3,2-dioxaborinane 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 1173294-92-2 (4-bromophenyl)(2-(pyridin-2-yl)phenyl)methanone 
• 333-47-1 1-bromo-4-(trifluoromethyl)thiobenzene 

Relevant articles and documents

Modular and highly stereoselective approach to all-carbon tetrasubstituted alkenes

A modular and completely stereoselective approach for the construction of all-carbon tetrasubstituted alkenes is described. It is based on the three-fold, sequential metal-catalyzed, cross-coupling functionalization of simple enolphosphate dibromide templates with carbon nucleophiles, affording tetrasubstituted alkenes as single isomers.

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

Oxidatively Induced Reductive Elimination: Exploring the Scope and Catalyst Systems with Ir, Rh, and Ru Complexes

Direct conversion of C-H bonds into C-C bonds is a promising alternative to the conventional cross-coupling reactions, thus giving rise to a wide range of efficient catalytic C-H functionalization reactions. Among the elementary stages in the catalytic C-