1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)-

1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)- - Names and Identifiers

Name	1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)-
Synonyms	-tert-Butyl 3-(((benzyloxy) (S)-1-Boc-3-(Cbz-amino)-piperidine (S)-1-N-BOC-3-N-(CBZ-AMINO)PIPERIDINE tert-butyl (3S)-3-(benzyloxycarbonylamino)piperidine-1-carboxylate (S)-tert-Butyl 3-(((benzyloxy)carbonyl)aMino)piperidine-1-carboxylate (S)-3-BENZYLOXYCARBONYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 3-(phenylmethoxycarbonylamino)-1-piperidinecarboxylic acid tert-butyl ester (3S)-3-[[(Phenylmethoxy)carbonyl]amino]-1-piperidinecarboxylic acid tert-butyl ester 1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)-
CAS	1002360-09-9

1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)- - Physico-chemical Properties

Molecular Formula	C18H26N2O4
Molar Mass	334.41
Density	1.15
Boling Point	471.6±44.0 °C(Predicted)
pKa	12.05±0.20(Predicted)
Storage Condition	2-8°C

1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)- - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
HS Code	29333990

1-Piperidinecarboxylicacid, 3-[[(phenylmethoxy)carbonyl]amino]-,1,1-dimethylethyl ester, (3S)- - Introduction

(S)-1-Boc-3-(Cbz-amino)-piperidine is an organic compound with the chemical formula C17H24N2O3. It is a white crystalline solid, stable at room temperature. The compound has a certain toxicity, should avoid contact with the skin and inhalation.

(S)-1-Boc-3-(Cbz-amino)-piperidine is commonly used in organic synthesis, especially as an important intermediate in drug synthesis. It can be used to synthesize other ligands or compounds for the synthesis of new drug molecules. It can also be used as a catalyst and expansion agent.

The method for preparing (S)-1-Boc-3-(Cbz-amino)-piperidine can be achieved by introducing an N-protecting group (Boc) and a C- protecting group (Cbz) into piperidine. One common method is by reacting piperidine with methyl chloroformate to form N-formylpiperidine, which is then reacted with ethyl 2-chloroacetate to form the (Cbz) amino group.

When using or handling (S)-1-Boc-3-(Cbz-amino)-piperidine, pay attention to proper laboratory practices and wear appropriate protective equipment, such as gloves and safety glasses. Keep away from open flames and heat sources, and avoid inhalation or direct skin contact. Waste generated during disposal shall be disposed of in accordance with local regulations.