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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, 3-cyano-, 1,1-dimethylethyl ester, (3S)-

N#C[C@H]1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 3-cyano-, 1,1-dimethylethyl ester, (3S)-
CAS Number: 915226-39-0
Product Number: AG00GRJ1(AGN-PC-0OMPTL)
Synonyms:
MDL No:
Molecular Formula: C11H18N2O2
Molecular Weight: 210.2728

Identification/Properties

Computed Properties
Molecular Weight:
210.277g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
210.137g/mol
Monoisotopic Mass:
210.137g/mol
Topological Polar Surface Area:
53.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
285
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-N-Boc-3-Cyanopiperidine, a versatile chemical compound, plays a crucial role in chemical synthesis processes. Its unique structure and properties make it an essential reagent in various synthetic routes for the production of pharmaceuticals, agrochemicals, and other fine chemicals. This compound is particularly valued for its ability to act as a chiral building block, aiding in the creation of new compounds with specific stereochemistry.(S)-1-N-Boc-3-Cyanopiperidine is utilized in asymmetric synthesis strategies to introduce chirality into organic molecules, enabling the creation of enantiomerically pure compounds. Its Boc (tert-butyloxycarbonyl) protecting group ensures selective reactions at specific positions, allowing for precise control over the stereochemistry of the final product. Additionally, the cyano group present in the molecule serves as a versatile functional group that can participate in a variety of reactions, further expanding the synthetic possibilities.In peptide chemistry, (S)-1-N-Boc-3-Cyanopiperidine is commonly employed for the synthesis of peptide derivatives and other bioactive molecules. Its compatibility with solid-phase peptide synthesis techniques makes it a valuable tool for constructing peptide chains with high efficiency and purity. The chiral nature of this compound also enables the production of peptide analogs with enhanced biological activity or improved pharmacokinetic properties.Beyond peptide synthesis, (S)-1-N-Boc-3-Cyanopiperidine finds applications in the preparation of synthetic intermediates for the synthesis of complex natural products, heterocyclic compounds, and other structurally diverse molecules. Its versatility as a building block allows chemists to access a wide range of chemical space and design novel molecules with desired properties for drug discovery, materials science, and other research areas.