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| | 5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione Basic information |
| Product Name: | 5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione | | Synonyms: | 1-c)-1,2,4-dithiazole-3-thione,5,6-dihydro-3h-imidazo(;PESTICIDMETABOLIT,5,6-DIHYDRO-3H-IMIDAZO[2,1-C]-1,2,4-DITHIAZOLE-3-THIONE;endodan;endodan50wp;etem;ethylenebisthiurammonosulfide;ethylenethiocarbamylsulfide;ethylenethiurammonosulfide | | CAS: | 33813-20-6 | | MF: | C4H4N2S3 | | MW: | 176.28 | | EINECS: | 251-684-4 | | Product Categories: | | | Mol File: | 33813-20-6.mol | ![5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione Structure](CAS/GIF/33813-20-6.gif) |
| | 5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione Chemical Properties |
| Melting point | 122.5°C | | density | 1.479 (estimate) | | refractive index | 1.5000 (estimate) | | solubility | Chloroform (Slightly, Heated), Ethyl Acetate (Slightly, Heated) | | form | solid |
| | 5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione Usage And Synthesis |
| Uses | Vegita is a metabolite of fungicide maneb (M163500). | | Production Methods | The commercial production of ETEM involves the cyclisation of ethylenediamine derivatives with sulphur-containing reagents, forming the imidazo-dithiazole ring system. This synthesis typically includes steps such as thiocarbamoylation and oxidative ring closure, often under controlled temperature and pH conditions to ensure high yield and purity. | | Mechanism of action | Contact action | | Pesticide Type | Fungicide; Metabolite |
| | 5,6-Dihydro-3H-imidazo[2,1-c]-1,2,4-dithiazole-3-thione Preparation Products And Raw materials |
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