169206-65-9

169206-65-9 - Names and Identifiers

Name	tert-butyl4-(2-methoxy-2-oxoethylidene)pipcarboxylate
Synonyms	Boc 4-Methoxycarbonylmethylene-piperidine tert-butyl4-(2-methoxy-2-oxoethylidene)pipcarboxylate tert-butyl 4-(2-methoxulidene)piperidine-1-carboxylate tert-Butyl4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylat tert-butyl 4-(2-methoxy-2-oxoethylidene)-1-piperidinecarboxylate tert-butyl 4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate tert-butyl4-(2-methoxy-2-oxoethylidene)piperidine-1-carboxylate(WX191795) 4-(2-methoxy-2-oxoethylidene)-1-piperidinecarboxylic acid tert-butyl ester 1-Piperidinecarboxylic acid, 4-(2-Methoxy-2-oxoethylidene)-, 1,1-diMethylethyl ester
CAS	169206-65-9

169206-65-9 - Physico-chemical Properties

Molecular Formula	C13H21NO4
Molar Mass	255.31
Storage Condition	2-8°C

169206-65-9 - Introduction

tert-butyl4-(2-methoxy-2-oxoethylidene)pipcarboxylate, also known as BTMEP, is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: BTMEP is a colorless to light yellow oily liquid.
-Solubility: It is soluble in organic solvents, such as ethanol, dimethylformamide and dichloromethane.

Use:
- BTMEP is a commonly used organic synthesis intermediate, which has a wide range of applications in the fields of medicine, pesticides, dyes and so on.
-It can be used as aminating reagent, nucleophilic reagent and alkali catalytic reagent in organic synthesis reaction.

Method:
The synthesis of-BTMEP is usually obtained by reacting 4-nitropiperidine and tert-butanol under acidic conditions.
-Then, under alkaline conditions, the product is reacted with Formic Anhydride to generate BTMEP.

Safety Information:
- BTMEP is an organic compound. You need to pay attention to protective measures during operation to avoid inhalation, contact with skin and eyes.
-If exposed or inhaled, rinse immediately with plenty of water and seek medical attention.
-During storage and handling, avoid contact with oxidants and strong acids to prevent dangerous reactions.

Last Update：2024-04-09 19:05:47