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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)-

1-BOC-3-AMINOINDAZOLE

Nc1nn(c2c1cccc2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-BOC-3-AMINOINDAZOLE
CAS Number: 1204298-58-7
Product Number: AG008UQ2(AGN-PC-0WAJ15)
Synonyms:
MDL No:
Molecular Formula: C12H15N3O2
Molecular Weight: 233.2664

Identification/Properties

Computed Properties
Molecular Weight:
233.271g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
233.116g/mol
Monoisotopic Mass:
233.116g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
301
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


The tert-Butyl 3-amino-1H-indazole-1-carboxylate is a versatile compound commonly utilized in chemical synthesis for its unique reactivity and structural properties. This specialized chemical plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials due to its ability to serve as a key building block in the synthesis of various complex organic molecules.In chemical synthesis, tert-Butyl 3-amino-1H-indazole-1-carboxylate is often employed as a starting material for the preparation of diverse heterocyclic compounds. Its functional groups and steric hindrance make it a valuable precursor in the formation of biologically active molecules, such as pharmaceutical drugs and biochemical probes. Furthermore, its versatility allows for the introduction of specific functionalities or substituents, enabling chemists to tailor the properties of the final product to meet desired specifications.Additionally, tert-Butyl 3-amino-1H-indazole-1-carboxylate serves as a crucial intermediate in the synthesis of various organometallic complexes and coordination compounds. Its unique structure and reactivity make it an essential component in the construction of molecular architectures with specific electronic and optical properties, pivotal in the design of materials for advanced technological applications.Overall, the use of tert-Butyl 3-amino-1H-indazole-1-carboxylate in chemical synthesis highlights its significance as a valuable tool for achieving synthetic goals in the development of diverse chemical compounds with potential applications across multiple industries.