1. Home
  2. spiro[1,4-dihydroquinoline-3,4'-piperidine]-2-one;hydrochloride

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)-

spiro[1,4-dihydroquinoline-3,4'-piperidine]-2-one;hydrochloride

O=C1Nc2ccccc2CC21CCNCC2.Cl Request for Quotation
Chemical Name: spiro[1,4-dihydroquinoline-3,4'-piperidine]-2-one;hydrochloride
CAS Number: 1175358-24-3
Product Number: AG0081HP(AGN-PC-0BL82F)
Synonyms:
MDL No:
Molecular Formula: C13H17ClN2O
Molecular Weight: 252.7399

Identification/Properties

Computed Properties
Molecular Weight:
252.742g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
252.103g/mol
Monoisotopic Mass:
252.103g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
284
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 1'H-Spiro[piperidine-4,3'-quinolin]-2'(4'H)-one hydrochloride serves as a valuable reagent in chemical synthesis due to its unique structure and reactivity. This compound has found wide applications as a versatile building block in the preparation of various heterocyclic compounds through cyclization reactions. Additionally, its spirocyclic core provides structural diversity to the synthesized molecules, making it a useful tool in the design and synthesis of bioactive compounds and pharmaceutical intermediates. Furthermore, the spiro compound's presence in the structure imparts distinct pharmacological properties to the synthesized products, enhancing their potential applications in medicinal chemistry and drug discovery efforts.