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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)-

tert-butyl 7-fluoroindazole-1-carboxylate

Fc1cccc2c1n(nc2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 7-fluoroindazole-1-carboxylate
CAS Number: 1305320-59-5
Product Number: AG000UL8(AGN-PC-0JEK2G)
Synonyms:
MDL No: MFCD18911746
Molecular Formula: C12H13FN2O2
Molecular Weight: 236.2422

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-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


1-Boc-7-fluoro-1H-indazole is a versatile building block in chemical synthesis due to its unique properties and reactivity. As a Boc-protected fluorinated indazole derivative, it plays a crucial role in the synthesis of various biologically active compounds and pharmaceutical intermediates. Its application in organic chemistry is particularly valuable in the preparation of fluorinated heterocycles and drug candidates. Additionally, 1-Boc-7-fluoro-1H-indazole serves as a key starting material for the creation of novel fluorinated molecules with enhanced properties for medicinal and material science research. Its ability to introduce fluorine atoms into organic molecules makes it a valuable tool for designing new compounds with improved bioactivity and physicochemical properties. Furthermore, its versatility in functional group transformations and selective reactivity make it a valuable asset in the arsenal of synthetic chemists aiming to construct complex molecular structures efficiently and selectively.