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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)-

3-Iodotetrahydrofuran

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Chemical Name: 3-Iodotetrahydrofuran
CAS Number: 121138-01-0
Product Number: AG008UC7(AGN-PC-03KYOJ)
Synonyms:
MDL No:
Molecular Formula: C4H7IO
Molecular Weight: 198.0023

Identification/Properties

Computed Properties
Molecular Weight:
198.003g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
197.954g/mol
Monoisotopic Mass:
197.954g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
46.8
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


3-Iodotetrahydrofuran is a versatile chemical compound that finds wide application in organic synthesis. As a halogenated derivative of tetrahydrofuran, it serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and materials. In chemical synthesis, 3-Iodotetrahydrofuran can be utilized as a reactive intermediate in the formation of complex organic molecules. Its iodine atom is particularly valuable for introducing functional groups or initiating reactions that lead to the creation of more intricate chemical structures. The presence of the tetrahydrofuran ring provides a unique three-dimensional scaffold that can influence the stereochemistry of the final products.Furthermore, 3-Iodotetrahydrofuran's reactivity makes it a key reagent in cross-coupling reactions, where it can participate in forming carbon-carbon bonds with various nucleophiles or electrophiles. This ability to facilitate bond formation is crucial in the synthesis of natural products, pharmaceuticals, and other biologically active compounds.Overall, the application of 3-Iodotetrahydrofuran in chemical synthesis highlights its importance as a tool for constructing complex organic molecules with precise control over structure and functionality. Its versatile reactivity and unique structural properties make it a valuable asset in the toolkit of synthetic chemists.