benzyl spiro[1,2-dihydroindole-3,4'-piperidine]-1'-carboxylate


Chemical Name: benzyl spiro[1,2-dihydroindole-3,4'-piperidine]-1'-carboxylate
CAS Number: 167484-18-6
Product Number: AG001XET(AGN-PC-0NCQHE)
Synonyms:
MDL No:
Molecular Formula: C20H22N2O2
Molecular Weight: 322.4009

Identification/Properties


Computed Properties
Molecular Weight:
322.408g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
322.168g/mol
Monoisotopic Mass:
322.168g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
439
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

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Chemical Structure



Benzyl spiro[indoline-3,4'-piperidine]-1'-carboxylate is a versatile compound commonly used in chemical synthesis as a key building block. It serves as a crucial intermediate in the preparation of various biologically active molecules, pharmaceuticals, and agrochemicals. Its unique structure, containing a spirocyclic core and a benzyl ester group, imparts specific reactivity and selectivity in synthetic pathways.One notable application of Benzyl spiro[indoline-3,4'-piperidine]-1'-carboxylate is in the synthesis of spirocyclic compounds, which are important in medicinal chemistry for their diverse biological activities. By leveraging the structural motifs present in this compound, chemists can access a wide range of spirocycles with varying ring sizes and substitution patterns. These spirocycles exhibit promising pharmacological properties and are valuable candidates for drug discovery efforts.In addition, Benzyl spiro[indoline-3,4'-piperidine]-1'-carboxylate can also be utilized in the construction of complex natural products and heterocyclic compounds. Its strategic incorporation into synthetic routes enables efficient access to target molecules with high structural complexity and stereochemical diversity. Furthermore, the reactivity of the carboxylate functionality allows for further functionalization and derivatization, expanding the synthetic possibilities and enabling the development of novel chemical entities.Overall, the application of Benzyl spiro[indoline-3,4'-piperidine]-1'-carboxylate in chemical synthesis showcases its significance as a powerful tool for the efficient construction of diverse molecular architectures with synthetic and medicinal relevance.