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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-3-carboxylic acid, 5-fluoro-

OC(=O)c1n[nH]c2c1cc(F)cc2 Request for Quotation
Chemical Name: 1H-Indazole-3-carboxylic acid, 5-fluoro-
CAS Number: 1077-96-9
Product Number: AG003MQB(AGN-PC-003AEQ)
Synonyms:
MDL No:
Molecular Formula: C8H5FN2O2
Molecular Weight: 180.1359

Identification/Properties

Properties
MP:
299°C
BP:
445.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
180.138g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
180.034g/mol
Monoisotopic Mass:
180.034g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
224
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


The 5-Fluoro-1H-indazole-3-carboxylic acid is a versatile compound widely used in chemical synthesis for its unique reactivity and functional group compatibility. It serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. One of its key applications is as a starting material for the preparation of novel heterocyclic compounds with potential biological activities.In organic synthesis, 5-Fluoro-1H-indazole-3-carboxylic acid can undergo various transformations such as acylation, alkylation, and condensation reactions to introduce different functional groups at specific positions on the indazole ring. This flexibility allows chemists to design and synthesize complex molecules with tailored properties for specific applications. Additionally, the presence of the fluoro substituent on the indazole ring provides unique opportunities for further derivatization and modulation of the compound's physicochemical properties.Overall, the 5-Fluoro-1H-indazole-3-carboxylic acid plays a crucial role in the realm of chemical synthesis by enabling the construction of diverse molecular architectures with potential therapeutic or material science significance. Its utility and versatility make it a valuable tool for synthetic chemists seeking to explore new pathways for the creation of innovative compounds.