Welcome to LookChem.com Sign In|Join Free
  • or
[(E)-2-carboxyethenyl](triphenyl)phosphonium, with the molecular formula C24H20O2P, is a phosphonium salt featuring a carboxyethenyl group. This chemical compound is recognized for its utility as a reagent in organic synthesis, particularly in the creation of carbon-carbon bonds. Its strong basic properties render it suitable for a wide array of chemical reactions. Furthermore, its catalytic properties make it a valuable tool in specific reaction types and in the exploration of phosphonium salts within organophosphorus chemistry.
Usage:
Used in Organic Synthesis:
[(E)-2-carboxyethenyl](triphenyl)phosphonium is used as a reagent for the formation of carbon-carbon bonds, a critical process in creating complex organic molecules. Its ability to facilitate these bond formations makes it a valuable component in the synthesis of various organic compounds.
Used in Chemical Reactions:
Acting as a strong base, [(E)-2-carboxyethenyl](triphenyl)phosphonium is utilized in a range of chemical reactions where a strong basic environment is required. This attribute broadens its applicability across different areas of chemistry.
Used as a Catalyst:
In certain reactions, [(E)-2-carboxyethenyl](triphenyl)phosphonium serves as a catalyst, enhancing the rate of the reaction without being consumed in the process. This role is significant in optimizing reaction conditions and improving overall efficiency.
Used in Organophosphorus Chemistry:
The study of phosphonium salts, a subset of organophosphorus chemistry, often involves [(E)-2-carboxyethenyl](triphenyl)phosphonium. Its unique structure and properties make it an important compound for research and development in this field.
Used in Pharmaceutical Industry:
While not explicitly mentioned in the provided materials, given its role in organic synthesis and its potential applications in catalysis, it is plausible that [(E)-2-carboxyethenyl](triphenyl)phosphonium could also find use in the pharmaceutical industry, particularly in the development of new drugs and drug delivery systems.

22038-50-2

Post Buying Request

22038-50-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22038-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22038-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,3 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22038-50:
(7*2)+(6*2)+(5*0)+(4*3)+(3*8)+(2*5)+(1*0)=72
72 % 10 = 2
So 22038-50-2 is a valid CAS Registry Number.

22038-50-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-2-carboxyethenyl]-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names trans-2-Carboxy-vinyl-triphenylphosphoniumbromid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22038-50-2 SDS

22038-50-2Downstream Products

22038-50-2Relevant academic research and scientific papers

5(4H)-oxazolones. Part XI. Cycloaddition reaction of oxazolones and munchnones to triphenylvinylphosphonium salts as synthetic equivalents of alkynes

Clerici, Francesca,Gelmi, Maria Luisa,Trimarco, Pasqualma

, p. 5763 - 5774 (2007/10/03)

5(4H)-Oxazolones 1 and milnchnones 3 are reacted with triphenylvinylphosphonium bromide 2a to give, through a cycloaddition reaction, pyrrole derivatives 4a-d and 7a-c unsubstituted at C-3 and C-4. The use of substituted vinylphosphonium salts 2b,c and dipoles 1 and 3 allows the isolation of 3-methylpyrroles 4e, f and 7d,e and 3-pyrrolecarboxylic acids 9a-c, respectively. The cycloaddition reactions proceed with high regionelectivity because of the positive interaction of phosphonium group of 2 and carbonyl group of dipoles 1 and 3.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 22038-50-2