84040-16-4

Upstream product

• 16302-98-0 petivericin 
• 120-12-7 anthracene 

Downstream Products

• 93041-19-1 4-Phenyl-3,5-bis-trifluoromethyl-1H-pyrazole 
• 93041-17-9 1,4-Bis-trifluoromethyl-2,3-diaza-benzo[a]anthracene 
• 93041-18-0 2,3-Diaza-benzo[a]anthracene-1,4-dicarboxylic acid dimethyl ester 
• 93041-20-4 4-phenyl-1H-pyrazole-3,5-dicarboxylic acid dimethyl ester 
• 84040-25-5 S-α-(9,10-dihydro-9-anthryl)benzyl thioacetate 
• 38447-05-1 (2E,4E)-methyl 5-phenylpenta-2,4-dienoate 
• 150-60-7 dibenzyl disulphide 
• 120-12-7 anthracene 
• 84040-18-6 3,4-dimethyl-6-phenyl-5,6-dihydro-2H-thiopyran 
• 84040-22-2 (9,10-dihydro-9-anthryl)(phenyl)-methanethiol 
• 613-31-0 9,10-dihydroanthracene 

Relevant academic research and scientific papers

ADDITION REACTIONS OF SOME SIMPLE THIOALDEHYDES.

When generated at 100 deg C, aliphatic and aromatic thioaldehydes without electronic bias are shown to undergo addition reactions to both aliphatic and aromatic 1,3-dienes.The reaction is shown to have application in an intramolecular example.

The Generation and Trapping of Thiobenzaldehyde and Thioacetaldehyde

Thiobenzaldehyde and thioacetaldehyde have been generated by thermolysis of alkyl thiosulfinates under preparatively useful conditions and trapped with aromatic and aliphatic 1,3-dienes, the adducts with anthracene being convenient and high yielding sources of such thioaldehydes; thiobenzaldehyde has been shown to undergo the 'ene' reaction.