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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)-

1H-Inden-1-one, 2,3-dihydro-6-nitro-

[O-][N+](=O)c1ccc2c(c1)C(=O)CC2 Request for Quotation
Chemical Name: 1H-Inden-1-one, 2,3-dihydro-6-nitro-
CAS Number: 24623-24-3
Product Number: AG002OTO(AGN-PC-0JLYQD)
Synonyms:
MDL No:
Molecular Formula: C9H7NO3
Molecular Weight: 177.1568

Identification/Properties

Computed Properties
Molecular Weight:
177.159g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
177.043g/mol
Monoisotopic Mass:
177.043g/mol
Topological Polar Surface Area:
62.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
246
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-Nitro-2,3-dihydro-1H-inden-1-one is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound acts as an important building block in the synthesis of various organic molecules and pharmaceuticals. Its nitro group can undergo reduction reactions to yield different substituted indenone derivatives, which are valuable intermediates in the production of fine chemicals and biologically active compounds. Additionally, the presence of the dihydroindene moiety in 6-Nitro-2,3-dihydro-1H-inden-1-one provides a platform for creating complex molecular structures through further functionalization and modification. Its reactivity and structural properties make it a valuable tool in the synthesis of diverse organic compounds with potential applications in drug discovery, materials science, and various other fields of chemistry.