Tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate, with CAS number 203662-51-5, is a chemical compound characterized by its piperidine core structure, which is a six-membered ring containing one nitrogen atom. This compound features a tert-butyl ester group, contributing to its lipophilicity and stability. The presence of a hydroxy group and an allyl substituent (prop-2-en-1-yl) on the piperidine ring enhances its reactivity and potential for further chemical modifications. The hydroxy group can participate in hydrogen bonding, influencing the compound's solubility and interaction with biological systems. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Its synthesis and characterization would typically involve standard organic chemistry techniques, including esterification and functional group transformations. Overall, tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate represents a versatile scaffold for further exploration in various chemical and biological applications.

tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate

203662-51-5: Tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate, with CAS number 203662-51-5, is a chemical compound characterized by its piperidine core structure, which is a six-membered ring containing one nitrogen atom. This compound features a tert-butyl ester group, contributing to its lipophilicity and stability. The presence of a hydroxy group and an allyl substituent (prop-2-en-1-yl) on the piperidine ring enhances its reactivity and potential for further chemical modifications. The hydroxy group can participate in hydrogen bonding, influencing the compound's solubility and interaction with biological systems. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for research in medicinal chemistry. Its synthesis and characterization would typically involve standard organic chemistry techniques, including esterification and functional group transformations. Overall, tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate represents a versatile scaffold for further exploration in various chemical and biological applications.

CAS 203662-51-5

tert-butyl 4-hydroxy-4-(prop-2-en-1-yl)piperidine-1-carboxylate

1-Piperidinecarboxylic acid, 4-hydroxy-4-(2-propen-1-yl)-, 1,1-dimethylethyl ester

Ref: IN-DA00291Y

1-Boc-4-allyl-4-hydroxypiperidine

Ref: 54-OR1020970

tert-Butyl 4-allyl-4-hydroxypiperidine-1-carboxylate

Ref: 10-F465116