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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-(Cyclobutylethynyl)-3-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

Fc1nn(c2c1cc(C#CC1CCC1)cc2)C1CCCCO1 Request for Quotation
Chemical Name: 5-(Cyclobutylethynyl)-3-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole
CAS Number: 1365889-99-1
Product Number: AG00123H(AGN-PC-0WAKN0)
Synonyms:
MDL No:
Molecular Formula: C18H19FN2O
Molecular Weight: 298.3547

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
298.361g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
298.148g/mol
Monoisotopic Mass:
298.148g/mol
Topological Polar Surface Area:
27A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
466
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Cyclobutylethynyl)-3-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it an essential building block in the production of various advanced materials and pharmaceuticals. The presence of both a fluorine atom and a cyclobutyl ring in the molecule imparts distinctive properties that are valuable in organic synthesis. In particular, this compound is employed in the construction of complex molecular architectures through cross-coupling reactions, ring-closing reactions, and other transformations. Its incorporation in drug discovery and development also showcases its significance as a key intermediate in the preparation of potentially bioactive compounds with diverse pharmacological properties.