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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-Fluoro-1H-indazole

Fc1ccc2c(c1)cn[nH]2 Request for Quotation
Chemical Name: 5-Fluoro-1H-indazole
CAS Number: 348-26-5
Product Number: AG00349J(AGN-PC-0WAM6F)
Synonyms:
MDL No: MFCD04972877
Molecular Formula: C7H5FN2
Molecular Weight: 136.1264

Identification/Properties

Properties
MP:
119 - 121 °C
BP:
274.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
136.129g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
136.044g/mol
Monoisotopic Mass:
136.044g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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


5-Fluoro-1H-indazole is a valuable compound widely used in chemical synthesis due to its versatile reactivity and unique structural features. This heterocyclic molecule serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials. Its significance lies in its ability to participate in diverse chemical transformations, making it a valuable tool for organic chemists and researchers. In particular, 5-Fluoro-1H-indazole is commonly employed in the synthesis of bioactive small molecules, drug candidates, and functional materials. Its incorporation into molecular structures can lead to enhanced biological activity, improved selectivity, and altered physicochemical properties, making it an indispensable component in modern organic synthesis strategies. Furthermore, the presence of the fluorine substituent provides additional opportunities for fine-tuning the properties of the final products, further expanding the potential applications of 5-Fluoro-1H-indazole in chemical synthesis.