29476-14-0

Upstream product

• 29476-22-0 2,3-dihydro-2-phenyl-1,5-benzothiazepin-4(5H)-one 
• 73859-98-0 1-oxo-2-phenyl-1,2,3,5-tetrahydro-1λ⁴-benzo[b][1,4]thiazepin-4-one 

Downstream Products

• 29476-15-1 2,3-dihydro-4-methylthio-2-phenyl-1,5-benzothiazepine 
• 130337-10-9 2-Phenyl-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-one oxime 
• 129118-59-8 (2-Phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-hydrazine 
• 149492-89-7 1-Chloromethyl-5-phenyl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulene 
• 130337-41-6 2-phenyl-4-methyloxyimino-2,3-dihydro-5H-1,5-benzothiazepine 
• 130337-19-8 C₁₇H₁₆N₂O₂S 
• 130337-30-3 C₂₂H₁₈N₂O₂S 
• 130337-22-3 C₁₇H₁₃F₃N₂O₂S 
• 1483-30-3 2-styrylbenzothiazole 
• 118971-12-3 Isonicotinic acid N'-(2-phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-hydrazide 
• 118971-17-8 5-Phenyl-1-pyridin-4-yl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulene 
• 119003-98-4 5-Phenyl-1-pyridin-3-yl-4,5-dihydro-6-thia-2,3,10b-triaza-benzo[e]azulene 
• 118971-16-7 4,5-dihydro-5-phenyl-s-triazolo<3,4-d>-1,5-benzothiazepine 
• 118971-13-4 N'-(2-Phenyl-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl)-hydrazinecarboxylic acid ethyl ester 

Relevant academic research and scientific papers

Benzodiazepine analogues. Part 19.? 1H and 13C NMR spectroscopic studies of 2-phenyl-1,4- and 1,5-benzoheterazepinethione derivatives

Selected 1,4- and 1,5-benzoheterazepinones, prepared by the Schmidt rearrangement of flavanone analogues, were converted to the corresponding thiolactam derivatives using phosphorus pentasulfide. The proton and carbon chemical shifts of the thiolactam der

The Lawesson reagent as selective reducing agent for sulfoxides

Different functionalized sulfoxides can be selectively deoxygenated by Lawesson reagent to yield the corresponding sulfides in high amounts.

Oxazepines and thiazepines, XXV: Chemical transformations of 2,3-dihydro-1,5-benzothiazepin-4(5H)-ones

2,3-Dihydro-1,5-benzothiazepine-4(5H)-thiones 13-22 were prepared by the reaction of the appropriate 2,3-dihydro-1,5-benzothiazepin-4(5H)-ones with Lawesson's reagent. N-Acyl (23-25) and N-alkyl (26-28) derivatives have also been synthesized. Oxidation wi