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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)-

3H-Indazol-3-one, 6-fluoro-1,2-dihydro-

Fc1ccc2c(c1)[nH][nH]c2=O Request for Quotation
Chemical Name: 3H-Indazol-3-one, 6-fluoro-1,2-dihydro-
CAS Number: 862274-39-3
Product Number: AG004SPP(AGN-PC-04Q5A6)
Synonyms:
MDL No:
Molecular Formula: C7H5FN2O
Molecular Weight: 152.1258

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
152.128g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
152.039g/mol
Monoisotopic Mass:
152.039g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
185
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-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Fluoro-1H-indazol-3(2H)-one, also known as $name$, is a versatile compound that finds significant application in chemical synthesis. This compound serves as a valuable building block in the creation of various organic compounds due to its unique structural properties. In organic synthesis, $name$ is commonly employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine substituent imparts distinct reactivity and functionality, allowing for precise control over bond formation and stereochemistry. By strategically incorporating $name$ into synthetic routes, chemists can access a wide range of structurally diverse molecules with enhanced biological activities and desirable properties.