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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phosphonium, triphenyl(2-phenylethyl)-, bromide

c1ccc(cc1)CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-] Request for Quotation
Chemical Name: Phosphonium, triphenyl(2-phenylethyl)-, bromide
CAS Number: 53213-26-6
Product Number: AG003TO5(AGN-PC-0NBUG9)
Synonyms:
MDL No: MFCD02684953
Molecular Formula: C26H24BrP
Molecular Weight: 447.3465

Identification/Properties

Properties
MP:
216℃
Storage:
2-8℃;Inert atmosphere;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenethyltriphenylphosphonium bromide, known for its versatile range of applications in chemical synthesis, is a key reagent in organic chemistry. This compound is frequently utilized as a powerful Wittig reagent, enabling the efficient transformation of aldehydes and ketones into olefins through Wittig reactions. By facilitating the generation of carbon-carbon double bonds in a controlled manner, Phenethyltriphenylphosphonium bromide plays a crucial role in the construction of various organic molecules, including natural products, pharmaceuticals, and materials. Its compatibility with a wide array of functional groups and its ability to promote selective reactions make it a valuable tool for chemists seeking to access diverse chemical structures in their synthesis endeavors. In addition to its utility in Wittig reactions, Phenethyltriphenylphosphonium bromide can also be employed in other synthetic methodologies, demonstrating its significance as a versatile and reliable reagent in modern organic chemistry.