tert-Butyl diprop-2-ynylcarbamate

tert-Butyl diprop-2-ynylcarbamate - Names and Identifiers

Name	CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester
Synonyms	N-Boc-dipropargylamine tert-Butyl diprop-2-ynylcarbamate tert-butyl di(prop-2-yn-1-yl)carbaMate 2-Methyl-2-propanyl di-2-propyn-1-ylcarbamate Carbamic acid, di-2-propynyl-, 1,1-dimethylethyl ester (9CI) CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester
CAS	262418-92-8

tert-Butyl diprop-2-ynylcarbamate - Physico-chemical Properties

Molecular Formula	C11H15NO2
Molar Mass	193.2423
Storage Condition	Room Temprature
Use	Application of N-Boc-two propargyl amine can be used as an intermediate in organic synthesis and pharmaceutical intermediates, used in laboratory research and development process and the synthesis of pharmaceutical and chemical industry.

tert-Butyl diprop-2-ynylcarbamate - Introduction

CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester is an organic compound with the chemical formula C12H17NO2. It is a solid, colorless crystalline or crystalline powder, soluble in solvents, with a low melting point.

CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester is commonly used as an intermediate in organic synthesis, especially in the synthesis of nitrogen heterocyclic compounds and heterocyclic nitrogen-containing compounds. It can also be used as an activating reagent and a catalyst for participating in chiral synthesis reactions.

the preparation method of CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester is generally by reacting dipropargyl amine with bis (t-propyl) carbonate to generate CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester.

Regarding safety information, CarbaMic acid, N,N-di-2-propyn-1-yl-, 1,1-diMethylethyl ester should avoid contact with skin and eyes and avoid inhaling dust. Wear appropriate personal protective equipment such as gloves, masks and goggles during use. In addition, it should be stored in a dry and well-ventilated place, away from heat and fire sources, and prevent contact with oxidants and acids to avoid dangerous reactions.

Last Update：2024-04-10 22:29:15