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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)-

4,6-difluoro-1H-indazol-3-amine

Fc1cc(F)c2c(c1)[nH]nc2N Request for Quotation
Chemical Name: 4,6-difluoro-1H-indazol-3-amine
CAS Number: 1197193-24-0
Product Number: AG000PIS(AGN-PC-09T3XB)
Synonyms:
MDL No: MFCD13191634
Molecular Formula: C7H5F2N3
Molecular Weight: 169.1315

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
169.135g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
169.045g/mol
Monoisotopic Mass:
169.045g/mol
Topological Polar Surface Area:
54.7A^2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,6-Difluoro-1H-indazol-3-amine is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of a variety of complex molecules. Its fluorine substituents enhance its stability and influence its reactivity, making it a key component in the design and development of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 4,6-Difluoro-1H-indazol-3-amine can participate in a number of reactions to introduce functional groups or create new chemical bonds. For example, its amino group can undergo nucleophilic substitution reactions to replace the fluorine atoms with different functional groups, leading to the formation of diverse derivatives. Additionally, its indazole ring system offers opportunities for further modification through various synthetic strategies, such as Suzuki-Miyaura cross-coupling, Buchwald-Hartwig amination, and transition-metal-catalyzed C-H activation.Overall, the unique structure and reactivity of 4,6-Difluoro-1H-indazol-3-amine make it a valuable tool in the hands of synthetic chemists for the construction of complex molecules with diverse applications in medicinal chemistry, materials science, and beyond.