tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate

tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate - Names and Identifiers

Name	tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate
Synonyms	2-(Boc-aMino)-7-azaspiro[... 2-(Boc-aMino)-7-azaspiro[3.5]nonane 7-Azaspiro[3.5]nonane carbamic acid deriv tert-Butyl 7-azaspiro[3.5]non-2-ylcarbamate TERT-BUTYL 7-AZASPIRO[3.5]NONAN-2-YLCARBAMATE tert-butyl 7-azaspiro[3.5]nonan-2-ylcarbamate tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate 2-(tert-Butoxycarbonylamino)-7-azaspiro[3.5]nonane 7-Azaspiro[3.5]non-2-yl-carbamic acid tert-butyl ester CarbaMic acid, N-7-azaspiro[3.5]non-2-yl-, 1,1-diMethylethyl ester CarbaMic acid, 7-azaspiro[3.5]non-2-yl-, 1,1-diMethylethyl ester (9CI)
CAS	147611-03-8
InChI	InChI=1/C13H24N2O2/c1-12(2,3)17-11(16)15-10-8-13(9-10)4-6-14-7-5-13/h10,14H,4-9H2,1-3H3,(H,15,16)

tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate - Physico-chemical Properties

Molecular Formula	C13H24N2O2
Molar Mass	240.34
Density	1.06
Boling Point	362℃
Flash Point	173℃
Vapor Presure	0mmHg at 25°C
pKa	12.44±0.20(Predicted)
Storage Condition	2-8°C(protect from light)
Refractive Index	1.508

tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate - Introduction

tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate is an organic compound with the chemical formula C14H25N3O2. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate is a colorless liquid.
-Solubility: It is soluble in common organic solvents such as ethanol, ether and dichloromethane.
-Melting point and boiling point: Specific information about the melting point and boiling point of the compound may require more literature.

Use:
- tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate is often used as a catalyst in organic synthesis reactions.
-It can be used to construct nitrogen heterocyclic compounds and heterospiro compounds.
-This compound can be used in the synthesis of other organic molecules, such as drug synthesis.

Method:
The specific method for preparing the tert-butyl N-(7-azaspiro[3.5]nonan-2-yl)carbamate may vary depending on the research purpose, but the common synthetic route includes the following steps:
1. First, tert-butyl ester is functionalized through a series of steps.
2. Then, the produced product is reacted with a quinamine compound under appropriate conditions to form the target compound.

Safety Information:
-Common safe laboratory practices should be followed when handling or storing the compound.
-It may be irritating to the eyes and skin, so you should wear appropriate protective equipment, such as gloves and goggles, during operation.
-Before use, it is recommended to read the safety data sheet (SDS) of the compound to learn more about its safe use and handling.

Last Update：2024-04-09 21:01:54