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AB00628

17814-85-6 | (4-Carboxybutyl)triphenylphosphonium bromide

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $16.00 $11.00 -   +
5g 98% in stock $19.00 $13.00 -   +
25g 98% in stock $42.00 $30.00 -   +
100g 98% in stock $98.00 $69.00 -   +
500g 98% in stock $356.00 $249.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB00628
Chemical Name: (4-Carboxybutyl)triphenylphosphonium bromide
CAS Number: 17814-85-6
Molecular Formula: C23H24BrO2P
Molecular Weight: 443.3132
MDL Number: MFCD00011906
SMILES: OC(=O)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
NSC Number: 147756

 

Computed Properties
Complexity: 372  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 8  

 

 

Upstream Synthesis Route
  • (4-Carboxybutyl)triphenylphosphonium bromide is a key reagent widely utilized in chemical synthesis for its unique ability to act as a highly efficient phase transfer catalyst. This compound plays a crucial role in facilitating various organic reactions involving two immiscible phases, typically an organic and an aqueous phase. The presence of the carboxylic acid group provides enhanced water solubility, making this compound particularly useful in reactions where aqueous conditions are required.In chemical synthesis, (4-Carboxybutyl)triphenylphosphonium bromide is employed in a range of reactions including nucleophilic substitutions, alkylations, and ether formations. Its phase transfer catalysis property allows for the transfer of reactants from one phase to another, thereby enabling easier access to substrates that may not be soluble in the reaction medium. This leads to improved yields and selectivity in a variety of organic transformations.Moreover, the triphenylphosphonium moiety in this compound enhances the stability of reaction intermediates and helps accelerate the rate of certain chemical reactions. The versatility of (4-Carboxybutyl)triphenylphosphonium bromide in facilitating complex synthetic pathways makes it a valuable tool for synthetic chemists in pharmaceutical, agrochemical, and material science research.
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