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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-(methoxycarbonyl)phenyl]methyl]triphenyl-, bromide

COC(=O)c1ccc(cc1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-] Request for Quotation
Chemical Name: Phosphonium, [[4-(methoxycarbonyl)phenyl]methyl]triphenyl-, bromide
CAS Number: 1253-46-9
Product Number: AG003L1P(AGN-PC-0KKQ41)
Synonyms:
MDL No:
Molecular Formula: C27H24BrO2P
Molecular Weight: 491.3560

Identification/Properties

Properties
MP:
258-260°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
491.365g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
490.07g/mol
Monoisotopic Mass:
490.07g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
475
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound [4-(Methoxycarbonyl)benzyl](triphenyl)phosphonium bromide is a versatile reagent widely used in chemical synthesis. It serves as a key building block in organic chemistry reactions due to its unique properties and reactivity.This compound is commonly employed as a powerful methylating agent in various organic transformations. Its ability to transfer a methyl group to other organic molecules makes it valuable in the synthesis of complex organic compounds. Additionally, [4-(Methoxycarbonyl)benzyl](triphenyl)phosphonium bromide is utilized in the preparation of phosphonium ylides, which are essential intermediates in the Wittig reaction for the synthesis of alkenes.Furthermore, this compound plays a crucial role in the modification of natural products and pharmaceutical compounds through methylation and alkylation reactions. Its high reactivity and compatibility with a wide range of functional groups make it a valuable tool for chemists working in medicinal chemistry and drug development.In summary, the application of [4-(Methoxycarbonyl)benzyl](triphenyl)phosphonium bromide in chemical synthesis extends to various organic reactions, including methylation, ylide formation, and modification of bioactive compounds, showcasing its importance in modern synthetic chemistry.