CAS 6309-59-7
:N-hydroxytetrahydro-4H-thiopyran-4-imine
Description:
N-hydroxytetrahydro-4H-thiopyran-4-imine, with the CAS number 6309-59-7, is a chemical compound characterized by its unique structure that includes a thiopyran ring and a hydroxylamine functional group. This compound typically exhibits properties associated with both heterocycles and nitrogen-containing compounds. It is likely to be a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of the hydroxylamine group suggests potential reactivity, particularly in nucleophilic addition reactions, and it may serve as a precursor or intermediate in organic synthesis. Additionally, the thiopyran ring contributes to its stability and may influence its solubility in various solvents. The compound's applications could span across pharmaceuticals, agrochemicals, or materials science, although specific uses may vary. As with many chemical substances, safety data and handling precautions should be considered, as it may pose health risks if not managed properly.
Formula:C5H9NOS
InChI:InChI=1/C5H9NOS/c7-6-5-1-3-8-4-2-5/h7H,1-4H2
SMILES:C1CSCCC1=NO
Synonyms:- 4H-Thiopyran-4-one, tetrahydro-, oxime
- N-(thian-4-ylidene)hydroxylamine
- synthesis-13-002
- Tetrahydrothiopyran-4-one oxiMe
- etrahydrothiopyran-4-one oxime
- dihydro-2H-thiopyran-4(3H)-one oxime
- NSC 41600
- See more synonyms
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Found 5 products.
Tetrahydrothiopyran-4-one oxime
CAS:Formula:C5H9NOSPurity:98%Color and Shape:SolidMolecular weight:131.1961Tetrahydrothiopyran-4-one oxime
CAS:Tetrahydrothiopyran-4-one oximePurity:98%Molecular weight:131.20g/molTetrahydrothiopyran-4-one oxime
CAS:<p>Tetrahydrothiopyran-4-one oxime is a heterocyclic compound that contains a tetrahydrothiopyran ring. It is synthesized from dioxane and sulfur. Tetrahydrothiopyran-4-one oxime can be used to generate the corresponding tosylate through reaction with the corresponding alcohol. Tetrahydrothiopyran-4-one oxime can also be used as a building block for the synthesis of other heterocycles by cyclization or fragmentation reactions, such as cyclohexanone and stereoisomeric forms.</p>Formula:C5H9NOSPurity:Min. 95%Molecular weight:131.2 g/mol



