1. Home
  2. Benzaldehyde, 2-hydroxy-3,5-dinitro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzaldehyde, 2-hydroxy-3,5-dinitro-

O=Cc1cc(cc(c1O)[N+](=O)[O-])[N+](=O)[O-] Request for Quotation
Chemical Name: Benzaldehyde, 2-hydroxy-3,5-dinitro-
CAS Number: 2460-59-5
Product Number: AG002OPN(AGN-PC-0JLPG3)
Synonyms:
MDL No:
Molecular Formula: C7H4N2O6
Molecular Weight: 212.1165

Identification/Properties

Properties
MP:
68-70 °C(lit.)
BP:
301.5±42.0 °C(Predicted)
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
212.117g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
212.007g/mol
Monoisotopic Mass:
212.007g/mol
Topological Polar Surface Area:
129A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
282
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

Request for Quotation

Customer Feedback

Chemical Structure


3,5-Dinitrosalicylaldehyde is a versatile compound widely utilized in chemical synthesis for various applications. This compound serves as a key building block in the creation of complex organic molecules due to its unique chemical properties. In particular, 3,5-Dinitrosalicylaldehyde is commonly employed in the synthesis of heterocyclic compounds and pharmaceutical intermediates. Its ability to undergo a range of chemical reactions, such as nucleophilic addition and condensation, makes it a valuable tool for organic chemists seeking to design and produce novel compounds with specific biological activities. Additionally, its distinct nitro functional groups provide opportunities for further derivatization, allowing for the fine-tuning of molecular structures for desired properties. In summary, 3,5-Dinitrosalicylaldehyde plays a crucial role in advancing chemical synthesis methodologies and enabling the development of new molecules with potential applications in various industries.