1. Home
  2. 1-Piperidinecarboxylicacid, 3-(methylamino)-, 1,1-dimethylethyl ester,(3S)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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

CN[C@H]1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylicacid, 3-(methylamino)-, 1,1-dimethylethyl ester,(3S)-
CAS Number: 912368-73-1
Product Number: AG003CON(AGN-PC-0VRWJK)
Synonyms:
MDL No:
Molecular Formula: C11H22N2O2
Molecular Weight: 214.3046

Identification/Properties

Properties
BP:
340.442 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Moisture Sensitive
Refractive Index:
1.4600
Computed Properties
Molecular Weight:
214.309g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
214.168g/mol
Monoisotopic Mass:
214.168g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
223
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(S)-tert-Butyl 3-(methylamino)piperidine-1-carboxylate, also known by its chemical structure [INSERT CHEMICAL STRUCTURE], plays a crucial role in chemical synthesis as a chiral building block with remarkable versatility. This compound is commonly utilized in asymmetric synthesis as a key intermediate for the preparation of enantiomerically pure molecules. Its unique chiral structure imparts stereochemical control, allowing for the selective construction of complex molecules with defined spatial arrangements. In organic synthesis, (S)-tert-Butyl 3-(methylamino)piperidine-1-carboxylate serves as a valuable precursor for the synthesis of various biologically active compounds, pharmaceuticals, and agrochemicals. Its incorporation in synthetic routes enables the efficient production of enantiomerically enriched products, which are crucial for pharmaceutical development and other industries requiring optically pure compounds.Moreover, this compound's compatibility with a wide range of functional groups enhances its utility in diverse synthetic transformations, making it a versatile building block for the construction of structurally complex molecules. Its use in asymmetric synthesis has been instrumental in advancing the field of chiral chemistry and facilitating the production of enantiomerically pure compounds with high stereoselectivity. Overall, the application of (S)-tert-Butyl 3-(methylamino)piperidine-1-carboxylate in chemical synthesis exemplifies its significance as a valuable tool for achieving stereochemical control and preparing optically pure compounds of synthetic and pharmaceutical interest.