3543-98-4

Basic information

• Product Name: 2,2-dichloro-1,3-diphenylaziridine
• CAS NO: 3543-98-4
• Molecular Formula: C₁₄H₁₁Cl₂N
• Molecular Weight: 264.1498
• Mol File: 3543-98-4.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 377.6°C at 760 mmHg
• Flash Point: 182.1°C
• Density: 1.35g/cm³
• Vapor Pressure: 6.69E-06mmHg at 25°C
• Refractive Index: 1.662
• CAS DataBase Reference: 2,2-dichloro-1,3-diphenylaziridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dichloro-1,3-diphenylaziridine(3543-98-4)
• EPA Substance Registry System: 2,2-dichloro-1,3-diphenylaziridine(3543-98-4)

Safety Data

• Hazardous Substances Data: 3543-98-4(Hazardous Substances Data)

Usage

Chemical Family

2,2-dichloro-1,3-diphenylaziridine belongs to the aziridine family.

Physical State

It is a colorless liquid.

Odor

It has a strong, pungent odor.

Usage

It is used as a building block for organic synthesis and pharmaceutical production.

Application

It is also used as a reagent in the research and development of new chemical compounds.

Hazardous Nature

2,2-dichloro-1,3-diphenylaziridine is a hazardous substance.

Health Risks

It can cause skin and eye irritation, and prolonged exposure may lead to harmful health effects.

Safety Measures

Appropriate safety measures and handling procedures should be followed when working with this chemical.

Upstream product

• 56-23-5 tetrachloromethane 
• 538-51-2 benzylidene phenylamine 
• 116-16-5 1,1,1,3,3,3-hexachloro-propan-2-one 
• 67-66-3 chloroform 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 100-52-7 benzaldehyde 
• 62-53-3 aniline 
• 1749-19-5 phenyl(1-phenylethylidene)amine 
• 76772-99-1 Phenyl-[2,2,2-trichloro-1-phenyl-eth-(E)-ylidene]-amine 

Downstream Products

• 1393934-53-6 N-(hydroxyphenylmethyl)-N-phenylformamide 
• 142-04-1 aniline hydrochloride 
• 7476-66-6 methyl 2-chloro-2-phenylethanoate 
• 10295-54-2 Phenyl-chlor-essigsaeure-<4-nitro-anilid> 
• 69377-94-2 α-Chlor-α-phenyl-2-nitroacetanilid 
• 92884-97-4 2-Chloro-N-(4-chloro-2-nitro-phenyl)-2-phenyl-acetamide 
• 92884-95-2 Acetic acid (4-nitro-phenylcarbamoyl)-phenyl-methyl ester 
• 92884-96-3 Acetic acid (2-nitro-phenylcarbamoyl)-phenyl-methyl ester 
• 92884-98-5 Acetic acid (4-chloro-2-nitro-phenylcarbamoyl)-phenyl-methyl ester 
• 10295-39-3 α-Chlor-α-phenyl-N-phenyl-acetimidoylchlorid 
• 54755-95-2 2-oxo-1-phenyl-2-(phenylamino)ethyl acetate 
• 5110-77-0 N-phenyl-α-chlorophenylacetamide 
• 74-87-3 methylene chloride 
• 115-10-6 Dimethyl ether 

Relevant articles and documents

Ultrasonic assisted synthesis of gem-dichloroaziridine derivatives using Mg/CCl4 under neutral conditions

A novel and convenient method for synthesis of gem-dichloroaziridine derivatives was reported in that was utilized Mg powder with CCl4 for dichlorocarbene generation under ultrasonic irradiation. In this clean and efficient reaction procedure,

Nanocrystalline magnesium oxide as a solid base catalyst promoted one pot synthesis of gem-dichloroaziridine derivatives under thermal conditions

In this study, efficient and mild synthesis of gem-dichloroaziridines from Schiff bases in the presence of nanocrystalline magnesium oxide/chloroform as a novel source of dichlorocarbene intermediate under thermal conditions have been described. The react

Sonocatalyzed facile and mild one pot synthesis of gem-dichloroaziridine derivatives under alkaline conditions

In this research, rapid and efficient preparation of 2,2-dichloro-1,3- diarylaziridines through the reaction of Schiff base compounds with dichlorocarbene yielded in situ from chloroform and sodium hydroxide without any phase transfer catalyst under ultrasonic irradiation is described. The advantages of this reaction are very short reaction times, excellent product yields, simplicity of the method and high purity of products.