missing translation for 'onlineSavingsMsg'
Learn More

Benzyltriphenylphosphonium bromide, 98%

Product Code. 11460408
Change view
Click to view available options
Quantity:
10 g
50 g
250 g
Unit Size:
10g
250g
50g
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Product Code. Quantity unitSize
11460408 10 g 10g
11470408 50 g 50g
11480408 250 g 250g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
This item is not returnable. View return policy
Product Code. 11460408 Supplier Thermo Scientific Alfa Aesar Supplier No. B24567.09
Request Bulk or Custom Format

Please to purchase this item. Need a web account? Register with us today!

This item is not returnable. View return policy

CAS: 1449-46-3 | C25H22BrP | 433.33 g/mol

Benzyltriphenylphosphonium bromide is used as a reactant for stereoselective azidolysis of vinyl epoxides, enantioselective aziridination and Friedel-Crafts cyclization for asymmetric synthesis of dihydrexidine, biomimetic iron(III) mediated oxidative dimerization for synthesis of benzoquinone parvistemin A, enantioselective synthesis of syn-diarylheptanoids from D-glucose, preparation of β-amyloid plaque ligands and decarboxylative cyclopropanation. It react with 4-methyl-oxetan-2-one to produce 4-hydroxy-1-phenyl-1-(triphenyl-l5-phosphanylidene)-pentan-2-one.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Benzyltriphenylphosphonium bromide is used as a reactant for stereoselective azidolysis of vinyl epoxides, enantioselective aziridination and Friedel-Crafts cyclization for asymmetric synthesis of dihydrexidine, biomimetic iron(III) mediated oxidative dimerization for synthesis of benzoquinone parvistemin A, enantioselective synthesis of syn-diarylheptanoids from D-glucose, preparation of β-amyloid plaque ligands and decarboxylative cyclopropanation. It react with 4-methyl-oxetan-2-one to produce 4-hydroxy-1-phenyl-1-(triphenyl-l5-phosphanylidene)-pentan-2-one.

Solubility
Soluble in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 1449-46-3
Molecular Formula C25H22BrP
Molecular Weight (g/mol) 433.33
MDL Number MFCD00031707
InChI Key WTEPWWCRWNCUNA-UHFFFAOYSA-M
Synonym benzyltriphenylphosphonium bromide, bromo benzyl triphenylphosphorane, benzyltriphenylphosphanium bromide, phenylmethyl triphenylphosphonium bromide, benzyl triphenylphosphonium bromide, benzyl triphenyl phosphonium bromide, phosphonium, triphenyl phenylmethyl-, bromide, acmc-1ch0e, ksc491k3n
PubChem CID 2734970
IUPAC Name benzyl(triphenyl)phosphanium;bromide
SMILES [Br-].C(C1=CC=CC=C1)[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

Specifications

Melting Point 293°C to 298°C
Quantity 10 g
UN Number UN3464
Beilstein 3599867
Sensitivity Hygroscopic
Solubility Information Soluble in water.
Formula Weight 433.34
Percent Purity 98%
Chemical Name or Material Benzyltriphenylphosphonium bromide

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.