33696-10-5

Basic information

• Product Name: 2,4-diethyl-1-nitro-benzene
• Synonyms: 2,4-diethyl-1-nitro-benzene
• CAS NO: 33696-10-5
• Molecular Weight: 179.219
• Mol File: 33696-10-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,4-diethyl-1-nitro-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-diethyl-1-nitro-benzene(33696-10-5)
• EPA Substance Registry System: 2,4-diethyl-1-nitro-benzene(33696-10-5)

Safety Data

• Hazardous Substances Data: 33696-10-5(Hazardous Substances Data)

Upstream product

• 57442-24-7 1,3-diethyl-2-nitrobenzene 
• 141-93-5 m-diethylbenzene 
• 71-43-2 benzene 

Downstream Products

• 14719-47-2 2,4-dimethylmethylaniline 
• 210414-88-3 2,4-diethyl-6-bromo-aniline 
• 105905-71-3 3,5-diethyl-benzonitrile 
• 90267-03-1 1-bromo-3,5-diethylbenzene 
• 3854-90-8 3,5-diethylbenzoic acid 
• 33696-12-7 2-(5-Ethyl-2-nitro-phenyl)-propan-1-ol 
• 33696-13-8 2-(3-Ethyl-4-nitro-phenyl)-propan-1-ol 

Relevant articles and documents

THE CYCLISATION AND REARRANGEMENT OF THE NITRO DERIVATIVES OF AROMATIC HYDROCARBONS IN TRIFLUOROMETHANESULPHONIC ACID

A number of the nitro derivatives of aromatic hydrocarbons undergo reactions in trifluoromethanesulphonic acid at ca. 100 deg C in which either the nitro group undergoes a 1,3-rearrangement or cyclisation occurs to form an anthranil.The rates and product composition have been determined for reactions in which the subsituents ortho to the nitro group are methyl or ethyl.For the rearrangement reaction to occur, it appears necessary that the nitro group should be initially between two alkyl substituents.The cyclisation reaction is significant only when one of the ortho-substituents is an ethyl group.