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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 spiro[2H-indole-3,4'-piperidine]-1-carboxylate

O=C(N1CC2(c3c1cccc3)CCNCC2)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl spiro[2H-indole-3,4'-piperidine]-1-carboxylate
CAS Number: 676607-31-1
Product Number: AG0038I6(AGN-PC-045FM7)
Synonyms:
MDL No:
Molecular Formula: C17H24N2O2
Molecular Weight: 288.3847

Identification/Properties

Computed Properties
Molecular Weight:
288.391g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
288.184g/mol
Monoisotopic Mass:
288.184g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
396
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl spiro[indoline-3,4'-piperidine]-1-carboxylate is a versatile compound widely used in chemical synthesis. It serves as a key building block in the creation of various biologically active molecules and pharmaceuticals. This compound is particularly valued for its structural properties, which enable it to participate in a range of organic reactions, such as cycloadditions, oxidative transformations, and asymmetric synthesis processes. Its unique spirocyclic structure provides both stability and flexibility, making it an ideal candidate for the construction of complex molecular architectures. Researchers and chemists often utilize tert-Butyl spiro[indoline-3,4'-piperidine]-1-carboxylate as a valuable tool in the development of new drug candidates, agrochemicals, and materials with tailored properties. Its role in chemical synthesis extends to the creation of diverse heterocyclic compounds, natural product derivatives, and advanced intermediates that are crucial for advancing the frontiers of chemical research and innovation.