6794-94-1

Basic information

• Product Name: 1,2-diethyldiaziridine
• Synonyms: Einecs 229-864-9;1,2-diethyldiaziridine
• CAS NO: 6794-94-1
• Molecular Formula: C₅H₁₂N₂
• Molecular Weight: 100.16218
• EINECS: 229-864-9
• Mol File: 6794-94-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 95.3 °C at 760 mmHg
• Flash Point: 2.6 °C
• Appearance: /
• Density: 0.906 g/cm³
• Vapor Pressure: 45.6mmHg at 25°C
• Refractive Index: 1.462
• CAS DataBase Reference: 1,2-diethyldiaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-diethyldiaziridine(6794-94-1)
• EPA Substance Registry System: 1,2-diethyldiaziridine(6794-94-1)

Safety Data

• Hazardous Substances Data: 6794-94-1(Hazardous Substances Data)

Usage

General Description

1,2-Diethyldiaziridine is a chemical compound with the molecular formula C5H10N2. It is a synthetic organic compound that is used in the production of pharmaceuticals, dyes, and other organic chemicals. 1,2-Diethyldiaziridine is a clear, colorless liquid at room temperature and is highly flammable. It is also toxic and is a known irritant to the skin, eyes, and respiratory system. The chemical is not naturally occurring and is primarily produced in laboratory settings for specific industrial applications. It is important to handle 1,2-Diethyldiaziridine with caution and in accordance with safety guidelines to minimize the risks associated with its use.

InChI:InChI=1/C5H12N2/c1-3-6-5-7(6)4-2/h3-5H2,1-2H3

Upstream product

• 50-00-0 formaldehyd 
• 54280-83-0 N-Bromoethylamine 
• 75-04-7 ethylamine 
• 7779-27-3 1,3,5-triethyl-1,3,5-triazacyclohexane 
• 24948-82-1 N-chloroethylamine 

Downstream Products

• 863983-17-9 N-{[acetyl(ethyl)amino]methyl}-N-vinylacetamide 
• 52225-98-6 N-ethyl-N-(1-ethyl-4-oxo-3,3-diphenylazetidin-2-yl)-2,2-diphenylacetamide 

Relevant articles and documents

Kinetic and quantum chemical studies of the mechanism of formation of 1,2-dialkyldiaziridines

The regularities of AlkNHBr consumption in the reaction of formation of 1,2-dialkyldiaziridines in aqueous media were studied for the first time by UV spectrometry. The rate constants of particular steps of the reaction were estimated starting from the po

Syntheses of 1,2-di- and 1,2,3-trialkyldiaziridines

The reactions of 1,3,5-trialkylhexahydro-1,3,5-triazines with W-chloroalkylamines resulted in 1,2-dialkyldiaziridines, whereas the reactions of AT-chloroalkylamines or N,N-dichloroalkylamines with an excess of primary aliphatic amines gave 1,2,3-trialkyldiaziridines.

THE ROLE OF pH IN THE SYNTHESIS OF DIAZIRIDINES

The greatest yield in the synthesis of diaziridines from carbonyl compounds, amines, and aminating reagents in water is achieved at a specific pH, which shifts to less alkaline values with increasing -I effect of the substituents in the carbonyl compound and with increasing pKBH+ value of the amine.The role of pH is related to the conditions for the generation of an immonium from the intermediate α-aminocarbinol.The nuclear Overhauser effect was used to determine the orientation of the substituents in several diastereomers of the dialkyldiaziridines obtained.