66268-31-3

Basic information

• Product Name: 4H-1,3-Thiazin-2-amine, 5,6-dihydro-N-phenyl-, (Z)-
• CAS NO: 66268-31-3
• Molecular Formula: C10H12N2S
• Molecular Weight: 192.285
• Mol File: 66268-31-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 4H-1,3-Thiazin-2-amine, 5,6-dihydro-N-phenyl-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,3-Thiazin-2-amine, 5,6-dihydro-N-phenyl-, (Z)-(66268-31-3)
• EPA Substance Registry System: 4H-1,3-Thiazin-2-amine, 5,6-dihydro-N-phenyl-, (Z)-(66268-31-3)

Safety Data

• Hazardous Substances Data: 66268-31-3(Hazardous Substances Data)

Upstream product

• 7078-98-0 2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone 
• 6276-54-6 3-chloropropylamine hydrochloride 
• 103-72-0 phenyl isothiocyanate 
• 7647-01-0 hydrogenchloride 
• 3420-61-9 azetidine-1-carbothioic acid anilide 
• 29146-63-2 N-(3-hydroxypropyl)-N'-phenyl-thiourea 
• 62-53-3 aniline 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 
• 94407-77-9 S-phenylthiocarbamoyl-thiocarbonic acid O-ethyl ester 
• 80254-04-2 N-(3-aminopropyl)-5,6,8,9-tetrahydro-7-phenyldibenzoacridinium trifluoromethanesulphonate 

Downstream Products

• 3102-07-6 (5,6-dihydro-4H-[1,3]thiazin-2-yl)-methyl-phenyl-amine 
• 129663-55-4 2-N-(N'-methyl-N'-phenylcarbamoyl)anilino-5,6-dihydro-4H-1,3-thiazine 
• 129663-51-0 2-phenylimino-3-(N-methyl-N-phenylcarbamoyl)tetrahydro-1,3-thiazine 
• 34117-49-2 2,3,4-Trihydro-1,3-thiazino<3,2-a>benzimidazole 
• 554-68-7 triethylamine hydrochloride 
• 112108-92-6 3-(3-mercaptopropyl)-1-phenyl-2,4-dioxoimidazolidine 
• 129663-56-5 1-(5,6-Dihydro-4H-[1,3]thiazin-2-yl)-1,3,3-triphenyl-urea 
• 129663-52-1 2-[(Z)-Phenylimino]-[1,3]thiazinane-3-carboxylic acid diphenylamide 
• 13677-18-4 2-phenylimino-[1,3]thiazinane-3-carboxylic acid anilide 
• 129663-48-5 1-(5,6-Dihydro-4H-[1,3]thiazin-2-yl)-1,3-diphenyl-urea 
• 2933-39-3 3-Methyl-2-phenyl-imino-tetrahydro-1,3-thiazin 
• 13677-20-8 2-phenylimino-[1,3]thiazinane-3-carboxylic acid butylamide 
• 13677-19-5 2-phenylimino-[1,3]thiazinane-3-carboxylic acid benzylamide 
• 13677-25-3 3-benzoyl-2-phenylimino-[1,3]thiazinane 

Relevant articles and documents

Synthesis of Diaryl Diazaphosphonates via 1,6-Hydrophosphonylation of p-Quinone Methides with N-Heterocyclic Phosphine-Thioureas

A mild, efficient method for the synthesis of diaryl diazaphosphonates via 1,6-hydrophosphonylation/aromatization of p-quinone methides (p-QMs) with N-heterocyclic phosphine-thioureas has been developed. This transformation proceeds without any additive or catalyst under mild reaction conditions and tolerates a wide range of p-QMs. This methodology provides a straightforward access to diaryl phosphonate derivatives in good to excellent yields (up to 99%).

Synthesis of benzimidazole-fused heterocycles by intramolecular oxidative C-N bond formation using hypervalent iodine reagents

A straightforward approach by dehydrogenative C-N coupling between aryl C-H and N-H bonds using a hypervalent iodine reagent under mild conditions offers a versatile and convenient method for synthesizing various benzimidazole-fused heterocycles. Georg Th

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.