38023-75-5

Usage

InChI:InChI=1/C12H4Cl2O2/c13-7-3-1-5-9-6(12(16)11(5)15)2-4-8(14)10(7)9/h1-4H

Upstream product

• 4208-97-3 5,6-dichloroacenaphthene 
• 111601-77-5 2,2,5,6-tetrachloroacenaphthylen-1(2H)-one 
• 38023-76-6 1,2-dihydro-5,6-dichloroacenapthylene-1,2-diol 
• 33950-95-7 1,2-dibromo-5,6-dichloroacenaphthene 

Downstream Products

• 21265-87-2 5-(5,6-dichloro-2-oxo-acenaphthen-1-ylidene)-3-phenyl-2-thioxo-thiazolidin-4-one 
• 18331-87-8 5-(5,6-dichloro-2-oxo-acenaphthen-1-ylidene)-2-thioxo-3-p-tolyl-thiazolidin-4-one 
• 18331-94-7 5-(5,6-dichloro-2-oxo-acenaphthen-1-ylidene)-3-(4-methoxy-phenyl)-2-thioxo-thiazolidin-4-one 
• 18332-09-7 5-(5,6-dichloro-2-oxo-acenaphthen-1-ylidene)-3-(4-ethoxy-phenyl)-2-thioxo-thiazolidin-4-one 
• 18332-01-9 5-(5,6-dichloro-2-oxo-acenaphthen-1-ylidene)-3-(2-methoxy-phenyl)-2-thioxo-thiazolidin-4-one 

Relevant academic research and scientific papers

1,2-DERIVATIVES OF ACENAPHTYLENE. IV. COMPOSITION AND STRUCTURE OF THE PRODUCT FROM CHLORODEOXYGENATION OF 5,6-DICHLOROACENAPHTYLENE-1,2-DIONE

The action of phosphorus pentachloride on 5,6-dichloroacenaphthylene-1,2-dione leads to the formation of 2,2,5,6-tetrachloroacenaphthylene-1(2H)-one and not 1,1,2,2,5,6-hexachloroacenaphthene as believed earlier. 2,2,5,6-Tetrachloroacenaphthylen-1(2H)-one is dehalogenated by zinc dust to 5,6-dichloroacenaphthylen-1(2H)-one.When heated in 90percent sulfuric acid, it is hydrolyzed to 5,6-dichloroacenaphthylene-1,2-dione.