115754-62-6

Basic information

• Product Name: (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE
• Synonyms: (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE;Tributyl(1,3-dioxolan-2-ylmethyl)phosphonium Bromide
• CAS NO: 115754-62-6
• Molecular Formula: Br*C₁₆H₃₄O₂P
• Molecular Weight: 369.321
• Mol File: 115754-62-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 25-40 °C
• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE(115754-62-6)
• EPA Substance Registry System: (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE(115754-62-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 115754-62-6(Hazardous Substances Data)

Usage

Description

(DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE is a chemical compound that features a tributylphosphonium cation with a bromide anion. The cation includes a dioxalan-2-yl-methyl group, which is a six-membered cyclic organic compound characterized by the presence of two oxygen atoms within its ring structure. (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE is recognized for its role as a phase transfer catalyst in organic synthesis reactions, where it aids in the efficient movement of reactants between immiscible phases, such as organic solvents and aqueous solutions.

Uses

Used in Organic Synthesis:
(DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE is used as a phase transfer catalyst for facilitating the transfer of reactants between immiscible phases. It forms a complex with the reactants, enabling them to move more easily between an organic solvent and an aqueous phase, which is crucial for the success of certain organic synthesis reactions.
Used in Pharmaceutical Preparation:
In the pharmaceutical industry, (DIOXALAN-2-YL-METHYL)-TRIBUTYLPHOSPHONIUM BROMIDE is utilized in the preparation of various pharmaceuticals and organic compounds. Its ability to act as a phase transfer catalyst is particularly valuable in the synthesis of complex organic molecules that are often found in medicinal chemistry, thereby contributing to the development of new drugs and therapeutic agents.

Upstream product

• 4360-63-8 2-bromomethyl-1,3-dioxolane 
• 998-40-3 tributylphosphine 

Downstream Products

• 20711-53-9 p-hydroxy-cinnamaldehyde 
• 1429623-07-3 (E)-3-(5-(2,6-diphenyl-4H-pyran-4-ylidenemethyl)thieno[3,2-b]thiophen-2-yl)acrylaldehyde 
• 925452-65-9 C₂₃H₂₁NO₂ 
• 250386-01-7 (2E)-3-[4-[ethyl[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]amino]phenyl]-propenal 
• 959850-79-4 (E)-1-(2-bromo-phenyl)-2-(2-[1,3]dioxolan-2-yl-vinyl)-1H-pyrrole 

Relevant articles and documents

Diferrocenyl molecular wires. the role of heteroatom linkers

Diferrocenyl molecular "wires", in which two ferrocenes are linked by a conjugated chain, allowing the communication of redox information between the ferrocenes, are a versatile platform on which to investigate notions of molecular conductivity. In this paper, we examine the role of heteroatoms=including O, P, S, and Se, as well as C atoms in various oxidation states=separated from the ferrocenes by intervening double bonds which minimize any steric effects. Surprisingly, oxygen is a better electronic mediator than sulfur, a phenomenon we attribute to superior molecular orbital overlap. These fundamental studies on redox coupling will help to guide the design of efficient organic conductors for organic electronics.