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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)-

5,6-difluoro-1H-indazole

Fc1cc2[nH]ncc2cc1F Request for Quotation
Chemical Name: 5,6-difluoro-1H-indazole
CAS Number: 944898-96-8
Product Number: AG00H6D1(AGN-PC-093R1X)
Synonyms:
MDL No:
Molecular Formula: C7H4F2N2
Molecular Weight: 154.1169

Identification/Properties

Properties
BP:
281.4±20.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
154.12g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
154.034g/mol
Monoisotopic Mass:
154.034g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


5,6-Difluoro-1H-indazole is a versatile compound that finds wide application in chemical synthesis. It serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and materials with diverse functionalities. The presence of fluorine atoms in its structure enhances its reactivity and imparts unique properties to the resulting products. In organic synthesis, 5,6-Difluoro-1H-indazole acts as a key intermediate in the preparation of complex molecules, enabling the introduction of fluorine-containing motifs for targeted purposes. Its compatibility with various reaction conditions and ability to participate in diverse transformations make it a valuable tool for chemists seeking to access novel compounds with enhanced properties. Whether employed in medicinal chemistry to develop new drugs or in material science to enhance material performance, 5,6-Difluoro-1H-indazole proves to be an indispensable component in the toolkit of synthetic chemists.