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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)-

1-Piperidinecarboxylic acid, 4-(1H-indol-1-yl)-, 1,1-dimethylethyl ester

O=C(N1CCC(CC1)n1ccc2c1cccc2)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 4-(1H-indol-1-yl)-, 1,1-dimethylethyl ester
CAS Number: 170364-89-3
Product Number: AG003JY1(AGN-PC-0071BK)
Synonyms:
MDL No:
Molecular Formula: C18H24N2O2
Molecular Weight: 300.3954

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
300.402g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
300.184g/mol
Monoisotopic Mass:
300.184g/mol
Topological Polar Surface Area:
34.5A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
396
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(1H-indol-1-yl)piperidine-1-carboxylate is a versatile compound that finds its application in chemical synthesis processes. Due to its unique structure and functional groups, this compound serves as a valuable building block in the creation of various complex molecules. Its presence in chemical reactions allows for the introduction of specific structural motifs and functionalities, enabling the synthesis of diverse organic compounds with desired properties. In the realm of organic chemistry, tert-Butyl 4-(1H-indol-1-yl)piperidine-1-carboxylate plays a crucial role in the preparation of biologically active molecules, pharmaceutical intermediates, and materials with tailored characteristics. Its utility in chemical synthesis paves the way for the development of new compounds and the exploration of novel chemical reactions.