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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, (iodomethyl)triphenyl-, iodide

IC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[I-] Request for Quotation
Chemical Name: Phosphonium, (iodomethyl)triphenyl-, iodide
CAS Number: 3020-28-8
Product Number: AG003AYI(AGN-PC-0NDR9W)
Synonyms:
MDL No:
Molecular Formula: C19H17I2P
Molecular Weight: 530.1210

Identification/Properties

Properties
MP:
260-266°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
530.128g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
529.916g/mol
Monoisotopic Mass:
529.916g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
253
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#:
-
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


(Iodomethyl)triphenylphosphonium iodide is a powerful and versatile reagent that finds wide application in organic chemical synthesis. This compound is commonly used as a methylene-transfer agent due to its ability to transfer a methyl group to various nucleophiles, leading to the formation of carbon-carbon bonds. Additionally, (Iodomethyl)triphenylphosphonium iodide is utilized in the synthesis of various pharmaceuticals, agrochemicals, and natural products, where the introduction of a methyl group is crucial for the desired chemical transformation. In summary, (Iodomethyl)triphenylphosphonium iodide serves as a key building block in organic synthesis, enabling the creation of complex molecules with enhanced efficiency and control.