Rel-1,1-Dimethylethyl N-[(3R,4R)-3-methyl-4-piperidinyl]carbamate, with the CAS number 473839-07-5, is a chemical compound characterized by its specific structural features that include a carbamate functional group and a piperidine ring. This compound is typically used in pharmaceutical applications, often as an intermediate in the synthesis of biologically active molecules. Its stereochemistry, indicated by the (3R,4R) configuration, suggests that it possesses chiral centers, which can influence its biological activity and interactions with biological targets. The presence of the dimethyl group contributes to its steric properties, potentially affecting its solubility and permeability. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, rel-1,1-Dimethylethyl N-[(3R,4R)-3-methyl-4-piperidinyl]carbamate is of interest in medicinal chemistry due to its potential therapeutic applications and the role of its structural characteristics in determining its efficacy and safety profile.

rel-1,1-Dimethylethyl N-[(3R,4R)-3-methyl-4-piperidinyl]carbamate

473839-07-5: Carbamic acid, N-[(3R,4R)-3-methyl-4-piperidinyl]-, 1,1-dimethylethyl ester, rel-, rel-1,1-Dimethylethyl N-[(3R,4R)-3-methyl-4-piperidinyl]carbamate, Carbamic acid, [(3R,4R)-3-methyl-4-piperidinyl]-, 1,1-dimethylethyl ester, rel-, trans-4-((tert-Butyloxycarbonyl)amino)-3-methylpiperidine

Please enquire for more information about trans-(3-Methyl-piperidin-4-yl)-carbamic acid tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

CAS 473839-07-5: rel-1,1-Dimethylethyl N-[(3R,4R)-3-methyl-4-piperidinyl]carbamate

trans-(3-Methyl-piperidin-4-yl)-carbamic acid tert-butyl ester

Ref: 3D-YTA83907

tert-Butyl N-[rel-(3R,4R)-3-methyl-4-piperidyl]carbamate

Ref: TR-B814800

Carbamic acid, [(3R,4R)-3-methyl-4-piperidinyl]-, 1,1-dimethylethyl ester, rel-

Ref: IN-DA00DPFI