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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-4-nitro-

O=C1CCc2c1cccc2[N+](=O)[O-] Request for Quotation
Chemical Name: 1H-Inden-1-one, 2,3-dihydro-4-nitro-
CAS Number: 24623-25-4
Product Number: AG002OTN(AGN-PC-0JLYQE)
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


4-Nitroindanone is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various organic compounds, making it a valuable tool for synthetic chemists. In particular, 4-Nitroindanone is commonly employed as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. Its structural features facilitate the introduction of diverse functional groups, enabling the modification and derivatization necessary for the development of novel compounds with desired biological activities. Additionally, 4-Nitroindanone can participate in various multistep synthetic schemes, acting as a pivotal intermediate in the construction of intricate molecular architectures. Its broad utility and compatibility with a range of synthetic methodologies make 4-Nitroindanone an essential component in the toolkit of organic chemists seeking to access diverse chemical space and develop innovative compounds for various applications.