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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)-

5-hydroxy-2-nitrobenzaldehyde

O=Cc1cc(O)ccc1[N+](=O)[O-] Request for Quotation
Chemical Name: 5-hydroxy-2-nitrobenzaldehyde
CAS Number: 42454-06-8
Product Number: AG003MSF(AGN-PC-0JKQQA)
Synonyms:
MDL No:
Molecular Formula: C7H5NO4
Molecular Weight: 167.1189

Identification/Properties

Properties
MP:
165-169 °C(lit.)
BP:
373°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Air Sensitive
Solubility:
Soluble in methanol.
Computed Properties
Molecular Weight:
167.12g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
167.022g/mol
Monoisotopic Mass:
167.022g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Hydroxy-2-nitrobenzaldehyde is a versatile compound commonly employed in chemical synthesis due to its unique properties and reactivity. This compound is a key intermediate in the production of various pharmaceuticals, dyes, and organic compounds. Its primary application lies in the synthesis of heterocyclic compounds, which are essential building blocks in medicinal chemistry and the pharmaceutical industry.In chemical synthesis, 5-Hydroxy-2-nitrobenzaldehyde is frequently utilized as a precursor for the construction of biologically active molecules with therapeutic potential. By undergoing various chemical transformations such as reduction, cyclization, or condensation reactions, this compound can be converted into diverse derivatives with specific functionalities and structures. These derivatives exhibit a wide range of pharmacological activities, making them valuable tools for drug discovery and development.Additionally, 5-Hydroxy-2-nitrobenzaldehyde plays a crucial role in the synthesis of organic pigments and dyes. Its ability to undergo selective modifications allows for the creation of colorants with different hues and properties, catering to a variety of industrial applications such as textiles, cosmetics, and food coloring.Overall, the versatility of 5-Hydroxy-2-nitrobenzaldehyde in chemical synthesis makes it an indispensable building block for the production of valuable compounds across multiple industries, contributing significantly to the advancement of pharmaceuticals, materials science, and other fields of research.