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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)-

6-Fluoro-3-iodo-1-methyl-1H-indazole

Fc1ccc2c(c1)n(C)nc2I Request for Quotation
Chemical Name: 6-Fluoro-3-iodo-1-methyl-1H-indazole
CAS Number: 1257535-15-1
Product Number: AG009Z69(AGN-PC-0WBOHL)
Synonyms:
MDL No:
Molecular Formula: C8H6FIN2
Molecular Weight: 276.0495

Identification/Properties

Computed Properties
Molecular Weight:
276.05g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
275.95597g/mol
Monoisotopic Mass:
275.95597g/mol
Topological Polar Surface Area:
17.8Ų
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
178
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


6-Fluoro-3-iodo-1-methyl-1H-indazole is a versatile compound that finds application in a variety of chemical synthesis processes. Its unique structure makes it a valuable building block for the synthesis of complex organic molecules and pharmaceuticals. This compound can undergo various reaction pathways to introduce functional groups at specific positions, enabling chemists to tailor the properties of the final product. In pharmaceutical research, 6-Fluoro-3-iodo-1-methyl-1H-indazole is often used as a key intermediate in the synthesis of potential drug candidates. Its selective reactivity and compatibility with different coupling reactions make it a valuable tool for organic chemists striving to develop novel compounds with promising biological activities.