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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, [(4-bromophenyl)methyl]triphenyl-, bromide

Brc1ccc(cc1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-] Request for Quotation
Chemical Name: Phosphonium, [(4-bromophenyl)methyl]triphenyl-, bromide
CAS Number: 51044-13-4
Product Number: AG003AYC(AGN-PC-0KK0GO)
Synonyms:
MDL No:
Molecular Formula: C25H21Br2P
Molecular Weight: 512.2160

Identification/Properties

Properties
MP:
270-273 °C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
512.225g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
511.973g/mol
Monoisotopic Mass:
509.975g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
378
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-Bromobenzyl)triphenylphosphonium bromide is a versatile chemical reagent commonly used in organic synthesis for its unique properties. This compound serves as an efficient and selective source of benzylic radicals in various synthetic transformations. Due to its ability to undergo homolytic cleavage under mild conditions, it is often employed in radical reactions, including radical couplings, cyclizations, and functional group interconversions. Additionally, (4-Bromobenzyl)triphenylphosphonium bromide can facilitate the introduction of benzyl groups into organic molecules through nucleophilic aromatic substitutions, enabling the efficient synthesis of various benzyl-substituted compounds. Its ease of handling and compatibility with a wide range of reaction conditions make it a valuable tool for chemists seeking to access structurally diverse and complex molecules in their synthetic endeavors.