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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)-

Spiro[1H-indene-1,4'-piperidin]-3(2H)-one, hydrochloride

O=C1CC2(c3c1cccc3)CCNCC2.Cl Request for Quotation
Chemical Name: Spiro[1H-indene-1,4'-piperidin]-3(2H)-one, hydrochloride
CAS Number: 231938-20-8
Product Number: AG00BHRG(AGN-PC-01ZL07)
Synonyms:
MDL No:
Molecular Formula: C13H16ClNO
Molecular Weight: 237.7252

Identification/Properties

Computed Properties
Molecular Weight:
237.727g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
237.092g/mol
Monoisotopic Mass:
237.092g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
268
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Spiro[indene-1,4'-piperidin]-3(2H)-one hydrochloride is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a key building block in the creation of various biologically active molecules, pharmaceuticals, and functional materials. Its unique spirocyclic structure contributes to its valuable chemical properties and reactivity in synthetic processes. In chemical synthesis, Spiro[indene-1,4'-piperidin]-3(2H)-one hydrochloride participates in the formation of complex molecular structures through strategic bond formations and diverse transformations. It is particularly prized for its ability to introduce specific functional groups and stereochemical elements into target molecules, enhancing the control and precision of synthetic routes. The compound's application in chemical synthesis extends to the creation of new drug candidates, agrochemicals, and advanced materials with tailored properties and functionalities.