21655-75-4

Upstream product

• 2971-23-5 1,1,1-trichloro-2,2-bis-(4-nitro-phenyl)-ethane 
• 116833-78-4 C₁₄H₈⁽²⁾HCl₃N₂O₄ 
• 67-64-1 acetone 
• 2971-22-4 2,2-bis(phenyl)-1,1,1-trichloroethane 
• 71-43-2 benzene 

Downstream Products

• 50296-99-6 4,4'-bis(acetamido)benzophenone 
• 611-98-3 4,4'-diaminobenzophenone 
• 77381-51-2 C₂₈H₂₂N₂O₄S₂ 
• 77381-56-7 Bis-(4-nitro-phenyl)-dithioacetic acid benzyl ester 
• 77381-52-3 C₂₀H₁₈N₂O₄S₂ 
• 77381-57-8 Bis-(4-nitro-phenyl)-dithioacetic acid allyl ester 
• 77381-49-8 C₁₆H₁₄N₂O₄S₂ 
• 110223-47-7 C₂₈H₂₂N₂O₄S₂ 
• 110223-44-4 C₂₁H₁₅ClN₂O₄S 
• 110223-48-8 C₂₈H₂₂N₂O₆ 
• 110223-46-6 C₂₁H₁₅ClN₂O₅ 
• 51348-08-4 1,1-dichloro-2,2-bis(4-aminophenyl)ethylene 
• 1033-26-7 4,4'-dinitrobenzophenone 

Relevant academic research and scientific papers

Kinetic and quantum chemical studies of the mechanism of dehydrochlorination of 2,2-diaryl-1,1,1-trichloroethanes with nitrite ions

The E2 mechanism has been proposed for the dehydrochlorination of 2,2-diaryl-1,1,1-trichloroethanes with nitrite ion, leading to 2,2-diaryl-1,1-dichloroethenes, on the basis of experimental kinetic study and quantum chemical simulation.

Kinetics and mechanism of the dehydrohalogenation of Ar2CHCX3 and Ar2CHCHX2 by strong N-bases

The kinetics and mechanism of the elimination reactions of 1,1,1- trifluoro-, 1,1,1-trichloro-, 1,1,1-tribromo-, 1,1-dichloro- and 1,1-dibromo- 2,2-bis(4-nitrophenyl)ethanes and two strong N-bases: 1,5,7- triazabicyclo[4.4.0]dec-5-ene (TBD) and 7-methyl-1

KINETICS AND ISOTOPE EFFECTS OF THE DEHYDROCHLORINATION OF 1,1,1-TRICHLORO-2,2-BIS-(4-NITROPHENYL)ETHANE WITH PIPERIDINE, PYRROLIDINE AND QUINUCLIDINE IN ACETONITRILE SOLVENT

Rate constants for the β-elimination reaction of HCl from 1,1,1-trichloro-2,2-bis-(4-nitrophenyl)ethane (I) promoted by piperidine, pyrrolidine, and quinuclidine bases in acetonitrile have been measured.Activation parameters are characterized by moderate

KINETICS, ISOTOPE EFFECTS AND MECHANISM OF THE REACTION OF SOME DINITROPHENYLETHANES WITH SODIUM PROPANETHIOLATE IN PROPANOL

The reaction between Ar2CHCF3, Ar2CHCCl3, Ar2CHCHCl2 (where Ar=O2NC6H4) and sodium propanethiolate in propanol has been investigated.The reaction of Ar2CHCF3 with sodium propanethiolate gave the following alkenes: Ar2C=CF2, Ar2C=CF(SPr) and Ar2C=C(SPr)2,

Kinetics and isotope effects of the β-elimination reactions of some 2,2-di(4-nitrophenyl)chloroethanes promoted by tetramethylguanidine in aprotic solvents

Rate constants for the β-elimination of HCl from 2,2-di(4-nitrophenyl)-1,1-dichloroethane (I) and 2,2-di(4-nitrophenyl)-1,1,1-trichloroethane (II) promoted by tetramethylguanidine in the aprotic solvents acetonitrile, tetrahydrofuran, and n-hexane have be