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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)-

Ethanone, 1-(5-hydroxy-2-nitrophenyl)-

Oc1ccc(c(c1)C(=O)C)[N+](=O)[O-] Request for Quotation
Chemical Name: Ethanone, 1-(5-hydroxy-2-nitrophenyl)-
CAS Number: 30879-49-3
Product Number: AG0031JA(AGN-PC-0JTIT2)
Synonyms:
MDL No:
Molecular Formula: C8H7NO4
Molecular Weight: 181.1455

Identification/Properties

Properties
MP:
146-147℃(Solv: ethyl acetate (141-78-6))
BP:
391.2 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
181.147g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
181.038g/mol
Monoisotopic Mass:
181.038g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
223
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(5-Hydroxy-2-nitrophenyl)ethanone is a versatile chemical compound that finds extensive application in various chemical synthesis pathways. This compound serves as a crucial building block in the synthesis of more complex chemical structures due to its unique reactivity and functional groups. Specifically, in chemical synthesis, 1-(5-Hydroxy-2-nitrophenyl)ethanone can be used as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals.Its reactive nitro and hydroxyl groups enable selective modifications through various chemical reactions such as reduction, nitration, and coupling reactions. By utilizing these functional groups, chemists can introduce specific molecular functionalities into target compounds, ultimately leading to the creation of novel chemical entities with desired properties.Additionally, the presence of the phenyl ring in 1-(5-Hydroxy-2-nitrophenyl)ethanone provides aromaticity, which further expands its synthetic utility in the construction of complex organic molecules. This compound's role in chemical synthesis underscores its importance as a pivotal starting material in the development of new materials and compounds across the chemical industry.