tert-butyl (1-iodopropan-2-yl)carbaMate

tert-butyl (1-iodopropan-2-yl)carbaMate - Names and Identifiers

Name	tert-butyl (1-iodopropan-2-yl)carbaMate
Synonyms	2-(Boc-amino)-1-iodopropane tert-butyl (1-iodopropan-2-yl)carbaMate tert-Butyl (2-iodo-1-Methylethyl)carbaMate (2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester
CAS	363599-44-4
InChI	InChI=1S/C8H16INO2/c1-6(5-9)10-7(11)12-8(2,3)4/h6H,5H2,1-4H3,(H,10,11)

tert-butyl (1-iodopropan-2-yl)carbaMate - Physico-chemical Properties

Molecular Formula	C8H16INO2
Molar Mass	285.12
Storage Condition	2-8℃

tert-butyl (1-iodopropan-2-yl)carbaMate - Introduction

tert-butyl (1-iodopropan-2-yl)carbaMate is an organic compound with the chemical formula C9H18INO2. Its properties are as follows:

Nature:
Appearance: White crystalline solid
Solubility: Soluble in organic solvents such as ethanol, methanol and chloroform, slightly soluble in water.

Use:
tert-butyl (1-iodopropan-2-yl)carbaMate is a commonly used organic synthesis reagent, commonly used in amino protection and the synthesis of amides and peptides. It has important applications in the field of drug synthesis and organic synthesis.

Preparation Method:
The preparation of tert-butyl (1-iodopropan-2-yl)carbaMate is generally obtained by reacting iodoalkanes with Boc-amino compounds. Specifically, iodopropane is reacted with a Boc-amino compound under the action of a base to produce the target product.

Safety Information:
The use of tert-butyl (1-iodopropan-2-yl)carbaMate should follow laboratory safety practices. It may be irritating to the eyes and skin and should be used to avoid contact. Wear appropriate protective equipment such as lab gloves, goggles and laboratory clothing during operation. Avoid fire and high temperature during storage and handling to prevent harmful gases.

Last Update：2024-04-09 02:00:45