1250998-93-6

1250998-93-6 - Names and Identifiers

Name	2-Methyl-2-propanyl 3-(iodomethyl)-2-oxa-8-azaspiro[4.5]decane-8-carboxylate
Synonyms	N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro[4.5]decane tert-butyl 3-(iodomethyl)-2-oxa-8-azaspiro[4.5]decane-8-carboxylate 2-Methyl-2-propanyl 3-(iodomethyl)-2-oxa-8-azaspiro[4.5]decane-8-carboxylate 3-(Iodomethyl)-2-oxa-8-azaspiro[4.5]decane-8-carboxylic acid tert-butyl ester Tert-Butyl 3-(Iodomethyl)-2-Oxa-8-Azaspiro[4.5]Decane-8-Carboxylate(WX102166) 2-methyl-2-propanyl 3-(iodomethyl)-2-oxa-8-azaspiro[4.5]decane-8- Carboxylate 2-Oxa-8-azaspiro[4.5]decane-8-carboxylic acid, 3-(iodomethyl)-, 1,1-dimethylethyl ester
CAS	1250998-93-6
EINECS	604-604-1
InChI	InChI=1S/C14H24INO3/c1-13(2,3)19-12(17)16-6-4-14(5-7-16)8-11(9-15)18-10-14/h11H,4-10H2,1-3H3

1250998-93-6 - Physico-chemical Properties

Molecular Formula	C14H24INO3
Molar Mass	381.25
Density	1.46
Boling Point	416.8±30.0 °C(Predicted)
pKa	-0.93±0.40(Predicted)
Storage Condition	Room Temprature

1250998-93-6 - Introduction

N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro [4.5] decane is an organic compound with the molecular formula C15H25INO2 and an iodomethyl group and an oxygen heterocycle in its structure. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: Colorless or light yellow solid
-Melting point: about 70-75 degrees Celsius
-Solubility: Soluble in common organic solvents, such as ether, alcohol, ketone, etc

Use:
- N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro [4.5] decane is usually used as an intermediate compound in organic synthesis and used in the synthesis of other organic compounds.
-It can be used as a protecting group or functional group transfer reagent in organic synthesis reactions.

Method:
the preparation method of N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro [4.5] decane is generally carried out by the following steps:
1. 3-bromopropanesulfonic acid and methyl iodide are added to a reaction vessel to generate 3-(iodomethyl) propanesulfonic acid.
2. Condensation reaction of 3-(iodomethyl) propanesulfonic acid with 2-butanol to generate N-BOC-3-(iodomethyl)-2-butyric acid.
3. finally, N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro [4.5] decane was obtained by the reaction of cuprous chloride and liquid ammonia.

Safety Information:
- N-BOC-3-(iodomethyl)-2-oxa-8-azaspiro [4.5] decane is unstable at room temperature and should be stored under low temperature and dry conditions.
-When using, please follow the correct laboratory procedures and bring appropriate personal protective equipment, such as laboratory gloves and protective glasses.
-This compound may be irritating and damaging to the eyes, skin and respiratory tract. Avoid direct contact or inhalation of its dust.
-If accidentally inhaled or exposed to the compound, rinse immediately with plenty of water and seek medical attention if necessary.

Last Update：2024-04-10 22:29:15