CAS 1003-04-9 Food Grade Tetrahydrothiophen-3-One Thiophene Chemical 99% High Purity
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x| IUPAC Name | Tetrahydrothiophen-3-one | Chemical Formula | C4H6OS |
|---|---|---|---|
| CAS Number | 1003-04-9 | Chemical Properties | Clear Light Yellow Liquid |
| Uses | Used For Blending Soft Drinks, Beverage, Meat Products, Confectionery, And Milk Product Flavors. | Boiling Point | 175 °C(lit.) |
| Highlight | CAS 1003-04-9 thiophene compound,High Purity Tetrahydrothiophen-3-one,Food Grade Tetrahydrothiophen-3-one |
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Tetrahydrothiophen-3-one is a sulfur-containing heterocyclic compound, often used in organic synthesis and pharmaceuticals.
| Synonyms | 3-Oxotetrahydrothiophene;3-Thiacyclopentanone;dihydro-3(2h)-thiophenon;Dihydro-3-Thiophenone;Thiolan-3-one;4,5-DIHYDRO-3(2H)-THIOPHENONE;3-THIOPHANONE;dihydrothiophen-3(2h)-one |
|---|---|
| CAS No. | 1003-04-9 |
| MF | C4H6OS |
| EINECS No. | 213-698-9 |
| FEMA No. | 3266 |
| Type | alliaceous |
| Usage | Used for blending soft drinks, beverage, meat products, confectionery, and milk product flavors |
| Purity | 99% |
| Odor | at 0.10 % in dipropylene glycol. garlic meaty green vegetables clams buttery |
| Appearance | Liquid |
Tetrahydrothiophen-3-one is primarily valued in industrial and research chemistry as a versatile synthetic building block. Its utility stems from its unique structure that combines a reactive ketone group with a saturated sulfur-containing ring (thioether).
This is the most significant role of Tetrahydrothiophen-3-one. It is not typically a final product but a crucial starting material or intermediate for synthesizing more complex, high-value molecules. Its chemical structure allows for transformations at two key sites:
- The Ketone Group (C=O): Highly reactive and can undergo a wide range of chemical reactions.
- The Thioether Group (-S-): Can be modified, most commonly through oxidation.
This is one of the most important applications. The molecule serves as a scaffold or precursor for creating pharmacologically active compounds.
- Core Structure in Active Molecules: The tetrahydrothiophene ring is a key structural motif (a "privileged scaffold") found in various drug candidates.
- Synthesis of Heterocyclic Compounds: It is used to build more complex ring systems that are common in medicines.
- Specific Examples: It is a key intermediate in the research and synthesis of compounds targeting a range of conditions, including:
- Central Nervous System (CNS) disorders.
- Anticancer agents.
- Enzyme inhibitors.
The compound is used to create novel pesticides and herbicides.
- Herbicides and Fungicides: Molecules containing the tetrahydrothiophene structure can exhibit potent herbicidal or fungicidal activity. Tetrahydrothiophen-3-one provides an efficient route to synthesize these molecules.
- Mode of Action: The sulfur atom can be crucial for the compound's ability to interact with biological targets in weeds or fungi.
