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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)-

Carbamic acid, (2-piperidinylmethyl)-, 1,1-dimethylethyl ester, (S)-

O=C(OC(C)(C)C)NC[C@@H]1CCCCN1 Request for Quotation
Chemical Name: Carbamic acid, (2-piperidinylmethyl)-, 1,1-dimethylethyl ester, (S)-
CAS Number: 139004-93-6
Product Number: AG001A04(AGN-PC-0PNPNH)
Synonyms:
MDL No:
Molecular Formula: C11H22N2O2
Molecular Weight: 214.3046

Identification/Properties

Computed Properties
Molecular Weight:
214.309g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
214.168g/mol
Monoisotopic Mass:
214.168g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
211
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl ((2S)-piperidin-2-ylmethyl)carbamate is a versatile compound used in chemical synthesis for its unique properties and applications. In organic chemistry, it is commonly employed as a protecting group for amines due to its stability under a variety of reaction conditions. This compound is particularly useful in the synthesis of complex organic molecules, where the selective protection of amine functional groups is required to prevent unwanted reactions. By strategically incorporating tert-Butyl ((2S)-piperidin-2-ylmethyl)carbamate into synthetic routes, chemists can control the reactivity of amine groups and efficiently manipulate the molecular structure to achieve desired target molecules. Its compatibility with a wide range of common reaction conditions and its ease of removal make it a valuable tool in the toolbox of synthetic chemists seeking to access diverse chemical structures.