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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)-

1H-Indole-1-carboxylic acid, 5-amino-, 1,1-dimethylethyl ester

Nc1ccc2c(c1)ccn2C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1H-Indole-1-carboxylic acid, 5-amino-, 1,1-dimethylethyl ester
CAS Number: 166104-20-7
Product Number: AG001WHZ(AGN-PC-00CA4G)
Synonyms:
MDL No:
Molecular Formula: C13H16N2O2
Molecular Weight: 232.2783

Identification/Properties

Computed Properties
Molecular Weight:
232.283g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
232.121g/mol
Monoisotopic Mass:
232.121g/mol
Topological Polar Surface Area:
57.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
298
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


1-Boc-5-Aminoindole, a versatile compound, plays a crucial role in chemical synthesis due to its unique properties and functionality. Its application in the field of organic chemistry is significant, as it serves as a valuable building block for the synthesis of various complex molecules. With its Boc-protected amine group and indole ring structure, this compound serves as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials. In chemical synthesis, 1-Boc-5-Aminoindole acts as a masked amine source, allowing for controlled and selective reactions. By utilizing this compound, chemists can introduce the desired amine functionality in a stepwise manner, facilitating the synthesis of diverse chemical structures. Additionally, the indole moiety provides a versatile platform for further functionalization, enabling the creation of novel compounds with tailored properties.Overall, the application of 1-Boc-5-Aminoindole in chemical synthesis offers researchers a valuable tool for the creation of complex molecules with precise control over their structure and function. Its strategic use in synthetic pathways leads to the development of innovative materials and bioactive compounds with potential applications in various industries.