1. Home
  2. tert-butyl 5-methylspiro[2H-indole-3,4'-piperidine]-1-carboxylate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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

Cc1ccc2c(c1)C1(CCNCC1)CN2C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 5-methylspiro[2H-indole-3,4'-piperidine]-1-carboxylate
CAS Number: 878376-82-0
Product Number: AG00IESM(AGN-PC-086FNU)
Synonyms:
MDL No:
Molecular Formula: C18H26N2O2
Molecular Weight: 302.4112

Identification/Properties

Computed Properties
Molecular Weight:
302.418g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
302.199g/mol
Monoisotopic Mass:
302.199g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
423
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

Request for Quotation

Customer Feedback

Chemical Structure


As a professional chemist, I can provide insight into the application of tert-Butyl 5-methylspiro[indoline-3,4'-piperidine]-1-carboxylate in chemical synthesis. This compound serves as a versatile building block in organic chemistry, particularly in the synthesis of complex heterocyclic systems. tert-Butyl 5-methylspiro[indoline-3,4'-piperidine]-1-carboxylate is strategically utilized for its spirocyclic structure, which offers unique steric and electronic properties that can influence reaction selectivity and product formation.In the realm of chemical synthesis, this compound is employed as a key intermediate for the construction of spirocyclic motifs, which are prevalent in pharmaceuticals, agrochemicals, and materials science. By incorporating tert-Butyl 5-methylspiro[indoline-3,4'-piperidine]-1-carboxylate into synthetic pathways, chemists can access a diverse array of structurally diverse compounds with potentially valuable biological or physical properties. The spirocyclic framework of this molecule can impart conformational rigidity and chiral centers, making it an attractive scaffold for generating molecular complexity and diversity.Furthermore, tert-Butyl 5-methylspiro[indoline-3,4'-piperidine]-1-carboxylate can act as a masked form of various reactive intermediates, enabling controlled transformations and enabling the construction of intricate molecular architectures with high efficiency and selectivity. Its presence in a synthetic route can facilitate the formation of multiple bonds and ring systems, leading to the streamlined synthesis of target molecules with desired biological or physicochemical properties. By judiciously incorporating this building block into synthetic strategies, chemists can access novel compounds and advance the frontiers of chemical synthesis and drug discovery.