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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-Indazole-7-carboxylicacid, 5-nitro-

[O-][N+](=O)c1cc2cn[nH]c2c(c1)C(=O)O Request for Quotation
Chemical Name: 1H-Indazole-7-carboxylicacid, 5-nitro-
CAS Number: 883290-89-9
Product Number: AG0089SP(AGN-PC-0K4J6Y)
Synonyms:
MDL No:
Molecular Formula: C8H5N3O4
Molecular Weight: 207.1430

Identification/Properties

Computed Properties
Molecular Weight:
207.14g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
207.028006g/mol
Monoisotopic Mass:
207.028006g/mol
Topological Polar Surface Area:
112Ų
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
290
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Nitro-1H-indazole-7-carboxylic acid is a versatile compound widely used in chemical synthesis due to its unique properties. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the preparation of a variety of pharmaceuticals, agrochemicals, and dyes.Its nitro group provides a reactive site for further functionalization, allowing for the creation of complex molecules with specific properties. Additionally, the indazole ring structure imparts unique aromatic and heterocyclic characteristics, making it a valuable scaffold in drug discovery and material science.In chemical synthesis, 5-Nitro-1H-indazole-7-carboxylic acid can be utilized as a starting material in the synthesis of various heterocyclic compounds, such as indazoles, triazoles, and benzimidazoles. Its presence in the synthesis pathway can enable the introduction of specific functional groups or stereochemical features, leading to the production of novel compounds with potential biological activities or other applications.Overall, 5-Nitro-1H-indazole-7-carboxylic acid plays a crucial role in the field of chemical synthesis, offering chemists a valuable tool for the creation of diverse and complex molecules with wide-ranging applications.