934342-48-0

Basic information

• Product Name: (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE
• Synonyms: (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE
• CAS NO: 934342-48-0
• Molecular Formula: C10H19BO3
• Molecular Weight: 198.07
• Mol File: 934342-48-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 229-230 °C(lit.)
• Flash Point: 214 °F
• Appearance: /
• Density: 0.933 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.4430(lit.)
• CAS DataBase Reference: (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE(934342-48-0)
• EPA Substance Registry System: (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE(934342-48-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 934342-48-0(Hazardous Substances Data)

Usage

General Description

"(E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE" is a chemical compound that consists of a boron atom and a dioxaboroane ring. It contains a methoxypropenyl group and four methyl groups, giving it a unique structure. (E)-2-(3-METHOXYPROPENYL)-4,4,5,5-TETRAMETHYL-(1,3,2)-DIOXABOROANE is commonly used in organic synthesis as a reagent for various reactions, including the synthesis of complex organic molecules and pharmaceuticals. It is known for its high reactivity and selectivity in promoting certain chemical transformations, making it a valuable tool in the field of organic chemistry.

Upstream product

• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 627-41-8 propargyl alcohol methyl ether 
• 73183-34-3 bis(pinacol)diborane 

Relevant articles and documents

Solvent- and metal-free hydroboration of alkynes under microwave irradiation

Boronic esters are versatile building blocks extensively used in organic chemistry and essential to a variety of coupling reactions. In this work, the hydroboration reactions of alkynes were performed without metal catalysts using concomitant microwave ir

One-Pot, Three-Step Synthesis of Cyclopropylboronic Acid Pinacol Esters from Synthetically Tractable Propargylic Silyl Ethers

Simple propargylic silyl ethers can be converted to complex cyclopropylboronic acid pinacol esters in an efficient one-pot procedure. Terminal acetylenes undergo a Schwartz's reagent catalyzed hydroboration; subsequent addition of further Schwartz's reage

Silver-catalyzed highly regioselective formal hydroboration of alkynes

A silver(I)-N-heterocyclic carbene complex has proven to be a potent catalyst for formal hydroboration of alkynes, providing a variety of borylalkenes in regio- and stereoselective manners. Under the silver catalysis, allenes also undergo regioselective hydroboration to give borylalkenes.