N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine

N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine - Names and Identifiers

Name	N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine
Synonyms	NSC 193472 AKOS BC-0427 N-(1-Adamantyl)ethylenediamin N-(1-ADAMANTYL)ETHYLENEDIAMINE 1-adamantyl(2-aminoethyl)amine N-(1-adamantyl)ethane-1,2-diamine 1-[N-(2-AMINOETHYL)AMINO]ADAMANTANE N-(Adamantan-1-yl)ethane-1,2-diamine N-Tricyclo[3.3.1.13,7]dec-1-yl-1,2-ethanediamine N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine 1,2-ethanediamine, N~1~-tricyclo[3.3.1.1~3,7~]dec-1-yl-
CAS	37818-93-2
EINECS	672-775-9
InChI	InChI=1/C12H22N2/c13-1-2-14-12-6-9-3-10(7-12)5-11(4-9)8-12/h9-11,14H,1-8,13H2

N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine - Physico-chemical Properties

Molecular Formula	C12H22N2
Molar Mass	194.32
Density	1,03 g/cm3
Boling Point	295.5±8.0 °C(Predicted)
Flash Point	154.2°C
Vapor Presure	0.00152mmHg at 25°C
pKa	10.72±0.20(Predicted)
Storage Condition	2-8℃
Refractive Index	1.5220-1.5250
MDL	MFCD02093421

N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)ethane-1,2-diamine - Introduction

N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine is an organic compound, also known as N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: A colorless to slightly yellow liquid.
-Molecular formula: C12H24N2.
-Molecular weight: 196.34g/mol.
-Solubility: Soluble in water and common organic solvents.

Use:
N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine has many applications:
-It can be used as a coordination reagent for the synthesis of complexes containing metal ions.
-It can be used as an amine group protection reagent in organic synthesis reactions.
-It can also be used as an intermediate in drug synthesis.

Preparation Method:
The preparation method of N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine is relatively complicated and generally includes the following steps:
-First, cyclopentane was synthesized starting from 1,4-cyclohexanedione.
-Then, cyclopentane is cyclized to adamantane through oxidation and reduction reactions.
-Finally, the obtained adamantane and ethylenediamine are subjected to an amination reaction to obtain N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine.

Safety Information:
N-(tricyclo[3.3.1.1~3,7 ~]dec-1-yl)ethane-1,2-diamine is an organic compound. The following safety precautions should be taken when using it:
-It may be irritating to the eyes, skin and respiratory system. Wear appropriate protective gloves, glasses and a mask when using it.
-Avoid contact with fire and heat. It is flammable and must not be stored or used with oxidizers.
-When using, ensure that it is carried out in a well-ventilated place to avoid inhaling its vapor for a long time.
-If accidental contact or inhalation, flush the affected area immediately with water and seek medical assistance if necessary.

Please note that this information is for informational purposes only. Consult a chemist or consult the literature for specific application and operational guidance.

Last Update：2024-04-09 21:01:54