17071-97-5

Upstream product

• 694-80-4 2-bromo-1-chlorobenzene 
• 34357-13-6 1,3λ⁴δ²,2,4-benzodithiadiazine 

Downstream Products

• 138415-81-3 3-(4-nitrophenyl)-1,2,4-benzotrithiin 
• 138415-83-5 3-(4-methoxyphenyl)-1,2,4-benzotrithiin 
• 138415-82-4 3-(2-Nitro-phenyl)-benzo[1,2,4]trithiine 
• 138415-79-9 3,3-Diphenyl-benzo[1,2,4]trithiine 
• 133559-89-4 Benzo[1,3]dithiol-2-ylidene-p-tolyl-amine 
• 59339-41-2 N-phenyl-2-imino-1,3-benzodithiole 
• 133559-93-0 Benzo[1,3]dithiol-2-ylidene-(4-chloro-phenyl)-amine 
• 133559-91-8 Benzo[1,3]dithiol-2-ylidene-(4-methoxy-phenyl)-amine 
• 133559-92-9 Benzo[1,3]dithiol-2-ylidene-(2-methoxy-phenyl)-amine 
• 138415-80-2 3-phenyl-1,2,4-benzotrithiin 
• 133559-90-7 Benzo[1,3]dithiol-2-ylidene-o-tolyl-amine 
• 152-18-1 O,O,O-trimethylthiophosphate 
• 92-85-3 Thianthrene 
• 186707-17-5 3-phenyl-1,2,4,5-benzotetrathiepin 

Relevant academic research and scientific papers

Polysulfane antitumor agents from o-benzyne. An odd-even alternation found in the stability of products o-C6H4Sx (x = 1-8)

Benzyne is shown to add elemental sulfur and give rise to a series of polysulfane compounds. A computational and experimental study is presented. Odd-membered o-C6H4Sx rings (x = 1-8), except x = 1, which suffers from ring strain, have enhanced stability compared to even-membered rings. The acquisition of odd-even data may shed new light, revealing patterns on polysulfane stability and structure.

New polysulfur-nitrogen heterocycles by thermolysis of 1, 3λ4δ2,2,4-benzodithiadiazines in the hydrocarbon and fluorocarbon series

In contrast to thermolysis of 1,3λ4δ2,2, 4-benzodithiadiazine (1) and its 5,6,7,8-tetrafluoro derivative 2 in dilute (10-3 M) hydrocarbon solutions, which leads to persistent 1,2,3-benzodithiazolyls in nearly quantitative