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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, methyltriphenyl-, chloride

C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-] Request for Quotation
Chemical Name: Phosphonium, methyltriphenyl-, chloride
CAS Number: 1031-15-8
Product Number: AG00390A(AGN-PC-0MV18X)
Synonyms:
MDL No:
Molecular Formula: C19H18ClP
Molecular Weight: 312.7730

Identification/Properties

Computed Properties
Molecular Weight:
312.777g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
312.083g/mol
Monoisotopic Mass:
312.083g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
235
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:
Danger
UN#:
3077
Hazard Statements:
H302+H312-H315-H318-H411
Precautionary Statements:
P273-P280-P305+P351+P338
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyltriphenylphosphonium chloride is a versatile reagent commonly used in chemical synthesis as a mild and efficient methylating agent. This compound plays a crucial role in organic transformations by facilitating the introduction of methyl groups onto various functional groups. Its unique properties make it particularly useful in reactions where traditional methylating agents may not be suitable or where harsh conditions are to be avoided. Additionally, Methyltriphenylphosphonium chloride is known for its compatibility with a wide range of substrates, making it a popular choice in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its ability to selectively methylate specific functional groups with high efficiency and excellent yield makes it a valuable tool for synthetic chemists looking to streamline complex reactions and achieve desired molecular modifications.