Tetrahydrothiophen-3-ol Supplier – 95% Purity Sulfur-Containing Heterocyclic Building Block | CAS 3334-05-2 | Finetech Industry Limited
1. Product Overview
Tetrahydrothiophen-3-ol (CAS No. 3334-05-2), also known as 3-hydroxytetrahydrothiophene or thiolan-3-ol, is a sulfur-containing heterocyclic alcohol used as a building block in organic synthesis and specialty chemical research.
Its molecular structure consists of a saturated five-membered sulfur-containing ring with a hydroxyl group attached at the 3-position. The combination of a cyclic thioether and an alcohol functional group provides opportunities for further chemical modification and the preparation of functionalized sulfur-containing compounds.
The hydroxyl group can participate in common alcohol-related transformations, including esterification, etherification, and oxidation under suitable reaction conditions. Meanwhile, the tetrahydrothiophene ring provides a stable sulfur-containing heterocyclic framework for molecular design and synthetic development.
Tetrahydrothiophen-3-ol is therefore a useful intermediate for research involving sulfur heterocycles, functionalized cyclic compounds, and specialty organic molecules.
Finetech Industry Limited supplies Tetrahydrothiophen-3-ol (CAS 3334-05-2) with a specified purity of 95%, as a light brown transparent liquid. Available packaging includes 1 g, 5 g, and 25 g for research and chemical synthesis requirements.
2. Product Specifications
| ParameterSpecification | |
| Product Name | Tetrahydrothiophen-3-ol |
| Product Number | FT-0650764 |
| CAS Number | 3334-05-2 |
| Synonyms | Thiolan-3-ol; 3-Hydroxytetrahydrothiophene; Tetrahydro-3-thiopheneol |
| Molecular Formula | C₄H₈OS |
| Molecular Weight | 104.17 g/mol |
| Appearance | Light brown transparent liquid |
| Purity | 95% |
| Available Packaging | 1 g, 5 g, 25 g |
3. Chemical Characteristics and Structural Features
Tetrahydrothiophen-3-ol belongs to the family of sulfur-containing saturated heterocyclic compounds. Its chemical structure combines a five-membered cyclic thioether ring with a secondary alcohol functionality.
Saturated Sulfur-Containing Heterocyclic Ring
The tetrahydrothiophene framework contains one sulfur atom within a five-membered saturated ring. Unlike aromatic thiophene, tetrahydrothiophene has a non-aromatic structure, providing different chemical and physical characteristics.
This sulfur-containing cyclic framework is useful in the preparation and investigation of functionalized heterocyclic compounds.
Hydroxyl Functional Group
The hydroxyl group at the 3-position provides a reactive site for further chemical transformations. Depending on the reaction system, it can be used in esterification, ether formation, oxidation, and other alcohol-related synthetic reactions.
These transformations allow the preparation of derivatives with different functional groups and molecular properties.
Versatile Intermediate for Molecular Modification
The coexistence of a cyclic thioether and a secondary alcohol makes Tetrahydrothiophen-3-ol a useful starting material for synthetic chemistry. Researchers can modify the hydroxyl group while retaining the sulfur-containing ring structure, supporting the development of structurally diverse compounds.
4. Research Applications of Tetrahydrothiophen-3-ol
4.1 Sulfur-Containing Heterocyclic Synthesis
Sulfur-containing heterocycles are important structural motifs in organic synthesis, pharmaceutical research, and specialty chemical development.
Tetrahydrothiophen-3-ol provides a five-membered sulfur-containing ring that can be incorporated into more complex molecular structures. Its hydroxyl functionality offers an additional reaction site for introducing substituents and preparing functionalized thiolane derivatives.
4.2 Pharmaceutical Intermediate Research
Sulfur-containing compounds are frequently investigated in medicinal chemistry and pharmaceutical intermediate development. Their structural diversity makes them useful in the design and synthesis of molecules with different physicochemical characteristics.
Tetrahydrothiophen-3-ol can serve as a starting material for preparing functionalized sulfur-containing intermediates and heterocyclic derivatives for further chemical and biological evaluation.
4.3 Alcohol Functionalization and Organic Synthesis
The secondary hydroxyl group in Tetrahydrothiophen-3-ol provides opportunities for a range of organic transformations.
Potential synthetic routes include:
- Esterification to prepare oxygen-functionalized derivatives.
- Etherification to introduce different alkyl or aryl substituents.
- Oxidation to investigate corresponding carbonyl-containing derivatives.
- Other functional group transformations for the preparation of specialized intermediates.
These reactions support research into the synthesis of functionalized cyclic sulfur compounds.
4.4 Medicinal Chemistry and Molecular Design
Sulfur-containing ring systems can be incorporated into molecular structures to explore changes in molecular shape, polarity, and physicochemical properties.
Tetrahydrothiophen-3-ol offers a compact heterocyclic scaffold with an accessible hydroxyl group. It can therefore be considered in medicinal chemistry research involving sulfur-containing molecular fragments, structural analogues, and functionalized heterocyclic compounds.
4.5 Specialty Chemical and Advanced Organic Research
Beyond pharmaceutical intermediate development, Tetrahydrothiophen-3-ol may be useful in specialty organic synthesis and research involving sulfur-containing functional materials.
Its combination of a cyclic thioether and hydroxyl group provides a starting point for investigating new synthetic pathways and preparing compounds with tailored functional characteristics.
5. Tetrahydrothiophen-3-ol Supply from Finetech Industry Limited
Finetech Industry Limited supplies Tetrahydrothiophen-3-ol (CAS 3334-05-2), with a specified purity of 95%, for research laboratories, chemical synthesis projects, and specialty chemical applications.
Product supply information:
- Purity: 95%.
- Appearance: Light brown transparent liquid.
- Molecular Formula: C₄H₈OS.
- Molecular Weight: 104.17 g/mol.
- Packaging Options: 1 g, 5 g, and 25 g.
- Application Areas: Sulfur heterocycle synthesis, pharmaceutical intermediate research, organic synthesis, and specialty chemical development.
Finetech Industry Limited provides flexible sourcing and packaging options to support customers working with specialized heterocyclic compounds and research chemicals.
For quotations, product availability, and additional quantity requirements, please contact our sales team.
6. Why Choose Finetech Industry Limited?
Finetech Industry Limited supplies specialty chemicals, pharmaceutical research intermediates, heterocyclic building blocks, and organic synthesis reagents to customers worldwide.
Our services focus on:
- A broad selection of specialty organic compounds and heterocyclic intermediates.
- Flexible packaging options for laboratory research and chemical development.
- Quality-oriented product sourcing and supply.
- Professional support for chemical procurement requirements.
- International shipping coordination for global customers.
We aim to provide reliable chemical supply, responsive communication, and professional service to support long-term cooperation with research organizations, pharmaceutical companies, and chemical businesses.
7. Contact Finetech Industry Limited
For quotations, product availability, or technical information regarding Tetrahydrothiophen-3-ol (CAS 3334-05-2), please contact Finetech Industry Limited.
Product Number: FT-0650764
Product Name: Tetrahydrothiophen-3-ol
CAS Number: 3334-05-2
Purity: 95%
Appearance: Light brown transparent liquid
Packaging: 1 g / 5 g / 25 g
Website: https://www.finetechnology-ind.com/
Contact Finetech Industry Limited for product quotations and international supply arrangements.