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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)-

Phosphonic acid, (iodomethyl)-, diethyl ester

ICP(=O)(OCC)OCC Request for Quotation
Chemical Name: Phosphonic acid, (iodomethyl)-, diethyl ester
CAS Number: 10419-77-9
Product Number: AG003PGS(AGN-PC-0JLU02)
Synonyms:
MDL No:
Molecular Formula: C5H12IO3P
Molecular Weight: 278.0252

Identification/Properties

Properties
BP:
112-114 °C (1 mmHg)
Storage:
2-8℃;
Form:
Liquid
Stability:
Light Sensitive
Refractive Index:
1.497-1.499
Computed Properties
Molecular Weight:
278.026g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
277.957g/mol
Monoisotopic Mass:
277.957g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
118
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Diethyl (iodomethyl)phosphonate is a versatile intermediate compound commonly used in chemical synthesis processes. This compound plays a crucial role in various reactions, particularly in the field of organic chemistry. One of its primary applications is as a reagent in the preparation of phosphorus-containing molecules.In chemical synthesis, Diethyl (iodomethyl)phosphonate serves as an effective source of the iodomethyl group, enabling the introduction of this functional group into organic compounds. This allows chemists to modify the structure of target molecules and incorporate iodine atoms into specific positions, which can significantly impact the properties and behavior of the resulting compounds.Furthermore, the presence of the phosphonate group in Diethyl (iodomethyl)phosphonate offers additional opportunities for diverse chemical transformations. This compound can participate in various reactions such as nucleophilic substitution, cross-coupling reactions, and transition-metal-catalyzed transformations, expanding its synthetic utility in the creation of complex organic molecules.Overall, Diethyl (iodomethyl)phosphonate is a valuable tool in chemical synthesis, enabling the efficient and controlled introduction of iodomethyl and phosphonate moieties into molecular structures, ultimately facilitating the discovery and development of new compounds with diverse applications in fields such as pharmaceuticals, materials science, and agrochemicals.