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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)-

2H-1-Benzopyran-2-one, 7-nitro-

O=c1ccc2c(o1)cc(cc2)[N+](=O)[O-] Request for Quotation
Chemical Name: 2H-1-Benzopyran-2-one, 7-nitro-
CAS Number: 19063-58-2
Product Number: AG002EPA(AGN-PC-0JU7CP)
Synonyms:
MDL No: MFCD09841089
Molecular Formula: C9H5NO4
Molecular Weight: 191.1403

Identification/Properties

Computed Properties
Molecular Weight:
191.142g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
191.022g/mol
Monoisotopic Mass:
191.022g/mol
Topological Polar Surface Area:
72.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
294
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


7-Nitrocoumarin is a versatile compound widely utilized in chemical synthesis as a key building block for various reactions and processes. This aromatic compound serves as a valuable starting material for the creation of diverse chemical structures due to its unique reactivity and functional groups. In the field of organic chemistry, 7-Nitrocoumarin is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its nitro group allows for facile manipulation and modification, enabling chemists to introduce new functionalities and complex structures through a series of synthetic transformations. Additionally, 7-Nitrocoumarin can participate in various organic reactions such as nucleophilic substitutions, reductions, and cyclizations, leading to the formation of a wide range of products with different properties and applications. This compound's versatility and reactivity make it an indispensable tool for synthetic chemists looking to access novel compounds and materials for various industrial and academic applications.