3420-40-4

Basic information

• Product Name: N-(3,4,5,6-TETRAHYDRO-1,3-THIAZIN-2-YLIDENE)ANILINE
• Synonyms: N-(3,4,5,6-TETRAHYDRO-1,3-THIAZIN-2-YLIDENE)ANILINE;2-Phenyliminotetrahydro-2H-1,3-thiazine;5,6-Dihydro-N-phenyl-4H-1,3-thiazine-2-amine;N-(3,4,5,6-Tetrahydro-2H-1,3-thiazine-2-ylidene)aniline;N-(Tetrahydro-2H-1,3-thiazine-2-ylidene)aniline;(E)-N-(1,3-thiazinan-2-ylidene)aniline;2-Phenylamino-5,6(4H)dihydro-1,3-thiazine;N-phenyl-5,6-dihydro-4H-1,3-thiazin-2-amine
• CAS NO: 3420-40-4
• Molecular Formula: C₁₀H₁₂N₂S
• Molecular Weight: 192.28068
• Mol File: 3420-40-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(3,4,5,6-TETRAHYDRO-1,3-THIAZIN-2-YLIDENE)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,4,5,6-TETRAHYDRO-1,3-THIAZIN-2-YLIDENE)ANILINE(3420-40-4)
• EPA Substance Registry System: N-(3,4,5,6-TETRAHYDRO-1,3-THIAZIN-2-YLIDENE)ANILINE(3420-40-4)

Safety Data

• Hazardous Substances Data: 3420-40-4(Hazardous Substances Data)

Usage

General Description

N-(3,4,5,6-Tetrahydro-1,3-thiazin-2-ylidene)aniline is a chemical compound with the molecular formula C9H11NS. It is a thiazine derivative with a substituted aniline group, and it is used in the synthesis of various pharmaceuticals and organic compounds. The compound is known for its potential biological and pharmacological activities, and it has been studied for its potential applications in drug discovery and development. N-(3,4,5,6-Tetrahydro-1,3-thiazin-2-ylidene)aniline is an important building block in organic chemistry, and it is utilized in the production of various functional materials and intermediates for the pharmaceutical and agrochemical industries.

Upstream product

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

Downstream Products

• 34117-49-2 2,3,4-Trihydro-1,3-thiazino<3,2-a>benzimidazole 
• 554-68-7 triethylamine hydrochloride 
• 129663-55-4 2-N-(N'-methyl-N'-phenylcarbamoyl)anilino-5,6-dihydro-4H-1,3-thiazine 
• 112108-92-6 3-(3-mercaptopropyl)-1-phenyl-2,4-dioxoimidazolidine 
• 129663-51-0 2-phenylimino-3-(N-methyl-N-phenylcarbamoyl)tetrahydro-1,3-thiazine 
• 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 
• 3102-07-6 (5,6-dihydro-4H-[1,3]thiazin-2-yl)-methyl-phenyl-amine 

Relevant articles and documents

A Bench-Stable Vilsmeier Reagent for in situ Alcohol Activation: Synthetic Application in the Synthesis of 2-Amino-2-Thiazolines

A robust, chemoselective direct condensation/cyclization of thioureas and amino alcohols is described. Employing a bench-stable Vilsmeier reagent, methoxymethylene- N, N -dimethyliminium methyl sulfate, the selective in situ activation of alcohols is achieved with high efficiency and broad functional-group tolerance. The reversible interaction of the Vilsmeier reagent with substrate was key to the success of this activation strategy.

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.