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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-Piperidinecarboxylicacid, 3-cyano-, 1,1-dimethylethyl ester, (3R)-

N#C[C@@H]1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylicacid, 3-cyano-, 1,1-dimethylethyl ester, (3R)-
CAS Number: 915226-44-7
Product Number: AG006LDS(AGN-PC-0VSQCE)
Synonyms:
MDL No:
Molecular Formula: C11H18N2O2
Molecular Weight: 210.2728

Identification/Properties

Properties
BP:
325.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
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:
H302-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


1-N-Boc-3-(R)-Cyanopiperidine is a versatile compound commonly utilized in chemical synthesis for its unique properties and functionalities. Known for its Boc (tert-butoxycarbonyl) protecting group, this molecular entity plays a crucial role in organic chemistry as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 1-N-Boc-3-(R)-Cyanopiperidine serves as a valuable intermediate due to its ability to protect sensitive functional groups and facilitate selective reactions. Its Boc protecting group shields reactive sites on molecules, allowing for controlled manipulation of desired chemical transformations. This compound's 3-(R)-Cyanopiperidine moiety enables the introduction of chirality, making it essential in the synthesis of enantiopure compounds with specific optical activity.Moreover, 1-N-Boc-3-(R)-Cyanopiperidine is often employed in the preparation of complex molecules such as pharmaceutical intermediates and natural products. Its structural features contribute to the efficient construction of molecular frameworks, enabling chemists to access diverse chemical space and design novel compounds with tailored properties.Overall, 1-N-Boc-3-(R)-Cyanopiperidine is a valuable asset in chemical synthesis, offering chemists a robust tool for the strategic assembly of intricate molecules and the realization of synthetic pathways leading to target compounds.