1175712-34-1

Basic information

• Product Name: Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate
• Synonyms: Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate
• CAS NO: 1175712-34-1
• Molecular Formula: C₁₆H₂₃BO₄
• Molecular Weight: 290.16242
• Mol File: 1175712-34-1.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate(1175712-34-1)
• EPA Substance Registry System: Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate(1175712-34-1)

Safety Data

• Hazardous Substances Data: 1175712-34-1(Hazardous Substances Data)

Usage

General Description

Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate is a chemical compound that is used in various industrial and research applications. It is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-oxygen bonds. Benzyl 3-(tetraMethyl-1,3,2-dioxaborolan-2-yl)propanoate is also used in the production of pharmaceuticals and agrochemicals. Additionally, it has been investigated for its potential use in other fields such as materials science and bioconjugation. The compound's unique structure and reactivity make it a valuable tool for chemists and researchers working in the fields of organic chemistry and chemical biology.

Upstream product

• 2495-35-4 benzylacrylate 
• 73183-34-3 bis(pinacol)diborane 
• 64-17-5 ethanol 
• 67-56-1 methanol 

Downstream Products

• 1243540-11-5 1-benzyl 4-tert-butyl 2-((4,4,5,5,-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)succinate 
• 1290145-52-6 8-(3-(benzyloxy)-3-oxopropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide 
• 1290145-63-9 (3-(benzyloxy)-3-oxopropyl)boronic acid 

Relevant articles and documents

Unexpected copper(II) catalysis: Catalytic amine base promoted β-borylation of α,β-unsaturated carbonyl compounds in water

Using bis(pinacolato)diboron, catalytic amounts of CuII, and various amine bases in water under atmospheric conditions at rt, acyclic and cyclic α,β-unsaturated ketones and esters are β-borylated in up to 98% yield. Mechanistic investigations u

Copper-Photocatalyzed Hydroboration of Alkynes and Alkenes

The photocatalytic hydroboration of alkenes and alkynes is reported. The use of newly-designed copper photocatalysts with B2Pin2 permits the formation a boryl radical, which is used for hydroboration of a large panel of alkenes and a

Catalyst-free chemoselective conjugate addition and reduction of α,β-unsaturated carbonyl compounds: Via a controllable boration/protodeboronation cascade pathway

A novel, efficient transition-metal-free and controllable boration/protodeboronation strategy has been developed for the chemoselective conjugate addition and 1,4-reduction of α,β-unsaturated carbonyl compounds. Without any metal-catalyst or base, a series of β-boration products of α,β-unsaturated carbonyl compounds was easily obtained in moderate to excellent yields in a mixed solvent of ethanol and water. The presence of a catalytic amount of Cs2CO3 can effectively induce further protodeboronation reaction towards 1,4-reduction products at higher reaction temperature. Therefore, by slightly changing the reaction conditions, the boration or reduction products of α,β-unsaturated carbonyl compounds can be controllably obtained. Mechanistic studies revealed that Cs2CO3 played the key role in activating the protodeboronation step. This transition-metal-catalyst-free and product controllable method provides a useful and eco-friendly tool for the highly chemoselective preparation of the β-boration products and 1,4-reduction products of α,β-unsaturated carbonyl compounds.