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2H-1,4-thiazene is a heterocyclic compound with the molecular formula C4H5NS. It is a member of the thiazene family, which consists of organic compounds containing a sulfur atom and a nitrogen atom in a five-membered ring. The structure of 2H-1,4-thiazene features a double bond between the sulfur and nitrogen atoms, with two hydrogen atoms attached to the nitrogen. 2H-1,4-thiazene is known for its aromatic properties and can be found in various pharmaceuticals and chemical reactions. Due to its reactivity, 2H-1,4-thiazene can undergo a range of chemical transformations, making it a versatile building block in organic synthesis.

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  • 290-56-2 Structure
  • Basic information

    1. Product Name: 2H-1,4-thiazene
    2. Synonyms: 2H-1,4-thiazene
    3. CAS NO:290-56-2
    4. Molecular Formula:
    5. Molecular Weight: 99.1564
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 290-56-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2H-1,4-thiazene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2H-1,4-thiazene(290-56-2)
    11. EPA Substance Registry System: 2H-1,4-thiazene(290-56-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 290-56-2(Hazardous Substances Data)

290-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290-56-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 290-56:
(5*2)+(4*9)+(3*0)+(2*5)+(1*6)=62
62 % 10 = 2
So 290-56-2 is a valid CAS Registry Number.

290-56-2Upstream product

290-56-2Downstream Products

290-56-2Relevant articles and documents

Catalytic removal of organic colorants from water using some transition metal oxide nanoparticles synthesized under sunlight

Shanker, Uma,Jassal, Vidhisha,Rani, Manviri

, p. 94989 - 94999 (2016)

Transition metal oxides (TMO) constitute a most amazing class of materials with a wide range of properties and applications; therefore, their synthesis using a green approach is a necessity. As such, sunlight irradiation was employed to synthesize various TMO nanostructures (ZnO, CuO, Co3O4, NiO and Cr2O3) using water as a solvent. Nanoparticles obtained with distinct morphologies, such as nanotubes (ZnO; 3O4; 45-90 nm), needle-shaped (NiO; 2-25 nm) and nanobeads (Cr2O3; ~17 nm) were confirmed by TEM analysis. The significance of the synthesis is in its quick approach with no thermal heat involvement, reusable catalyst, cost effectiveness and ability to fabricate almost uniformly distributed nanoparticles with small sizes. The potential of the synthesized nanoparticles was examined in the treatment of simulated water containing hazardous dyes: Alizarin Red S (ARS) + Methylene Blue (MB). Interestingly, in a short period of 180 min, 88.24% of the dye mixture was, for the most part, completely degraded using Cr2O3 nano-needles, followed by 87.96% (ZnO) > 86.86% (CuO) > 85.89% (NiO) > 80.35% (Co3O4), depending on the sizes of the respective TMO nanoparticles. This is also supported by the finding of small and non-toxic by-products such as but-2-enal, sulfur trioxide and benzoquinone. With high potential observed in the removal of dyes, TMO nanoparticles have a bright future with respect to their use as important adsorbents in waste water treatment. The advantage of the present work lies in the green synthesis of nanoparticles and their application in helping to make our environment green.

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