1170905-43-7

1170905-43-7 - Names and Identifiers

Name	3-[2-(Boc-amino)ethyl]azetidine Hydrochloride
Synonyms	3-[2-(BOC-AMINO)ETHYL]AZETIDINE HCL 3-Boc-aminoethylazetidine hydrochlordie 3-Boc-AMinoethylazetidine hydrochloride 3-[2-(Boc-aMino)ethyl]azetidine Hydrochloride 3-[2-(Boc-amino)ethyl]azetidine Hydrochloride tert-butyl 2-(azetidin-3-yl)ethylcarbamate HCl tert-Butyl 2-(3-azetidinyl)ethylcarbamate hydrochloride N-[2-(3-Azetidinyl)ethyl]-carbamic acid tert-butyl ester tert-butyl N-[2-(azetidin-3-yl)ethyl]carbamate hydrochloride
CAS	1170905-43-7

1170905-43-7 - Physico-chemical Properties

Molecular Formula	C10H21ClN2O2
Molar Mass	236.73894
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
MDL	MFCD09998720

1170905-43-7 - Preparation solution concentration reference

	1mg	5mg	10mg
1 mM	4.224 ml	21.12 ml	42.24 ml
5 mM	0.845 ml	4.224 ml	8.448 ml
10 mM	0.422 ml	2.112 ml	4.224 ml
5 mM	0.084 ml	0.422 ml	0.845 ml

Last Update：2024-01-02 23:10:35

1170905-43-7 - Introduction

3-[2-(Boc-amino)ethyl]azetidine Hydrochloride is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: A white crystalline solid
-Melting point: About 140-145 ° C
-Solubility: Soluble in water and common organic solvents, such as methanol and ether
-Stability: relatively stable under regular experimental conditions

Use:
3-[2-(Boc-amino)ethyl]azetidine Hydrochloride is commonly used in organic synthesis. It is a commonly used protecting group that can be used to protect amine groups. It is also commonly used in the synthesis of other organic compounds, such as pharmaceutical intermediates and biologically active molecules.

Preparation Method:
The preparation of 3-[2-(Boc-amino)ethyl]azetidine Hydrochloride is usually carried out by the following steps:
1. 2-boc-aminoethylamine is reacted with an appropriate amount of thionyl chloride to obtain 2-boc-aminoethylamine hydrochloride.
2. 2-boc-aminoethylamine hydrochloride is reacted with lithium cyanide to generate 3-(2-boc-aminoethyl) azetidine.
3. Finally, the obtained 3-(2-Boc-aminoethyl) azetidine is reacted with hydrochloric acid to obtain 3-[2-(Boc-amino)ethyl]azetidine Hydrochloride.

Safety Information:
- 3-[2-(Boc-amino)ethyl]azetidine Hydrochloride is an organic compound and should be operated according to laboratory safety procedures.
-Avoid inhalation, contact with skin and ingestion. In case of accidental contact, wash with plenty of water immediately and seek medical help.
-should be sealed and stored in a dry, cool place, away from fire and oxidant.
-Pay attention to personal protection during use and wear appropriate laboratory protective equipment, such as glasses, gloves and laboratory coats.

Last Update：2024-04-09 21:00:56