
CAS 907544-22-3
:1,1-Dimethylethyl N-[(3R,4R)-3-hydroxy-1-(phenylmethyl)-4-piperidinyl]carbamate
Description:
1,1-Dimethylethyl N-[(3R,4R)-3-hydroxy-1-(phenylmethyl)-4-piperidinyl]carbamate, with the CAS number 907544-22-3, is a chemical compound characterized by its complex structure, which includes a carbamate functional group and a piperidine ring. This compound features a chiral center, contributing to its stereochemistry, which is significant for its biological activity. It is typically used in pharmaceutical applications, particularly in the development of drugs targeting specific receptors or enzymes. The presence of the dimethyl group enhances its lipophilicity, potentially affecting its absorption and distribution in biological systems. Additionally, the hydroxyl group on the piperidine ring may participate in hydrogen bonding, influencing its interaction with biological targets. Overall, this compound exemplifies the intricate relationship between molecular structure and function, making it a subject of interest in medicinal chemistry and drug design.
Formula:C17H26N2O3
InChI:InChI=1S/C17H26N2O3/c1-17(2,3)22-16(21)18-14-9-10-19(12-15(14)20)11-13-7-5-4-6-8-13/h4-8,14-15,20H,9-12H2,1-3H3,(H,18,21)/t14-,15-/m1/s1
InChI key:InChIKey=BZTXNBTZLOOGHU-HUUCEWRRSA-N
SMILES:N(C(OC(C)(C)C)=O)[C@H]1[C@H](O)CN(CC2=CC=CC=C2)CC1
Synonyms:- Carbamic acid, N-[(3R,4R)-3-hydroxy-1-(phenylmethyl)-4-piperidinyl]-, 1,1-dimethylethyl ester
- Carbamic acid, [(3R,4R)-3-hydroxy-1-(phenylmethyl)-4-piperidinyl]-, 1,1-dimethylethyl ester
- 1,1-Dimethylethyl N-[(3R,4R)-3-hydroxy-1-(phenylmethyl)-4-piperidinyl]carbamate
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