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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[3H-indole-3,4'-piperidine], 1,2-dihydro-1'-(phenylmethyl)-

c1ccc(cc1)CN1CCC2(CC1)CNc1c2cccc1 Request for Quotation
Chemical Name: Spiro[3H-indole-3,4'-piperidine], 1,2-dihydro-1'-(phenylmethyl)-
CAS Number: 474538-99-3
Product Number: AG00DD7W(AGN-PC-013PAO)
Synonyms:
MDL No:
Molecular Formula: C19H22N2
Molecular Weight: 278.3914

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1'-Benzylspiro[indoline-3,4'-piperidine] is a versatile compound widely utilized in chemical synthesis as a key building block in the creation of various organic molecules. Its unique spirocyclic structure imparts distinctive properties that make it valuable in numerous synthetic applications. This compound serves as a crucial intermediate in the synthesis of complex molecules, such as pharmaceuticals, agrochemicals, and materials. Its structural features offer opportunities for structural diversification, enabling the construction of diverse molecular architectures efficiently. In addition, 1'-Benzylspiro[indoline-3,4'-piperidine] exhibits excellent reactivity and selectivity, making it a preferred choice for chemists in the development of novel compounds through strategic synthetic routes. Its versatile nature and synthetic utility make it an indispensable component in the toolkit of organic chemists globally.