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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)-

6-iodo-2,3-dihydroinden-1-one

Ic1ccc2c(c1)C(=O)CC2 Request for Quotation
Chemical Name: 6-iodo-2,3-dihydroinden-1-one
CAS Number: 14548-40-4
Product Number: AG001D2Z(AGN-PC-079S6F)
Synonyms:
MDL No:
Molecular Formula: C9H7IO
Molecular Weight: 258.0557

Identification/Properties

Computed Properties
Molecular Weight:
258.058g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
257.954g/mol
Monoisotopic Mass:
257.954g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
178
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


6-Iodo-1-indanone is a versatile compound that finds significant utility in various chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural properties. In the realm of organic synthesis, 6-Iodo-1-indanone is often employed as a key intermediate in the formation of complex molecules. By facilitating key bond formations and functional group manipulations, this compound enables chemists to access a diverse array of chemical structures with a high degree of precision. Its specific reactivity and compatibility with a wide range of reaction conditions make it a valuable tool for synthetic chemists seeking to access challenging molecular frameworks. In addition, the presence of the iodine moiety offers opportunities for further derivatization and diversification of the molecule, allowing for the fine-tuning of desired properties in the target compounds. Overall, the unique combination of structural features and reactivity make 6-Iodo-1-indanone an indispensable reagent in modern chemical synthesis strategies.