122947-54-0

Basic information

• Product Name: 1,5-dichloro-3-dichloromethyl-2-nitro-benzene
• Synonyms: 1,5-dichloro-3-dichloromethyl-2-nitro-benzene
• CAS NO: 122947-54-0
• Molecular Weight: 274.918
• Mol File: 122947-54-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,5-dichloro-3-dichloromethyl-2-nitro-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-dichloro-3-dichloromethyl-2-nitro-benzene(122947-54-0)
• EPA Substance Registry System: 1,5-dichloro-3-dichloromethyl-2-nitro-benzene(122947-54-0)

Safety Data

• Hazardous Substances Data: 122947-54-0(Hazardous Substances Data)

Upstream product

• 10203-08-4 3,5-dichlorobenzaldehyde 
• 56961-85-4 1,3-dichloro-5-dichloromethyl-benzene 
• 7697-37-2 nitric acid 
• 611-06-3 2,4-dichloronitrobenzene 
• 67-66-3 chloroform 
• 857619-05-7 α,α,3',5'-tetrachloro-2,2'-dinitro-deoxybenzoin 
• 59178-12-0 3,5-dichloro-2-nitrobenzaldehyde 

Downstream Products

• 59178-12-0 3,5-dichloro-2-nitrobenzaldehyde 

Relevant articles and documents

Dihalomethylation of Nitroarenes via Vicarious Nucleophilic Substitution of Hydrogen with Trihalomethyl Carbanions

Trichloro- and tribromomethyl carbanions generated by deprotonation of haloforms with potassium tert-butoxide in a THF-DMF mixture at ca. -70 deg C react with a variety of carbocyclic and heterocyclic nitroarenes according to the vicarious nucleophilic substitution scheme.The reaction provides an efficient and convenient way for the direct introduction of dihalomethyl substituents ortho and para to the nitro group, which in turn can be hydrolyzed to produce nitroaryl aldehydes.