TETRAHYDROTHIOPYRAN-4-OL 97
tetrahydro-2H-thiopyran-4-ol
CAS: 29683-23-6
Molecular Formula: C5H10OS
TETRAHYDROTHIOPYRAN-4-OL 97 - Names and Identifiers
| Name | tetrahydro-2H-thiopyran-4-ol |
| Synonyms | thian-4-ol Thiacyclohexane-4-ol Thiopyran-4-ol, tetrahydro- 4-Hydroxytetrahydrothiopyran Tetrahydro-2H-thiopyran-4-ol TETRAHYDROTHIOPYRAN-4-OL 97 tetrahydro-2H-thiopyran-4-ol 2H-thiopyran-4-ol, tetrahydro- 4-hydroxy-tetrahydro-2H-thiopyran |
| CAS | 29683-23-6 |
| InChI | InChI=1/C5H10OS/c6-5-1-3-7-4-2-5/h5-6H,1-4H2 |
TETRAHYDROTHIOPYRAN-4-OL 97 - Physico-chemical Properties
| Molecular Formula | C5H10OS |
| Molar Mass | 118.2 |
| Density | 1.148±0.06 g/cm3(Predicted) |
| Melting Point | 47-51 °C (lit.) |
| Boling Point | 70°C/0.05mmHg(lit.) |
| Flash Point | >230°F |
| Vapor Presure | 0.026mmHg at 25°C |
| pKa | 14.56±0.20(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Refractive Index | 1.55 |
TETRAHYDROTHIOPYRAN-4-OL 97 - Risk and Safety
| UN IDs | UN 3335 |
| WGK Germany | 3 |
| Hazard Class | IRRITANT |
TETRAHYDROTHIOPYRAN-4-OL 97 - Introduction
tetrahydro-2H-thiopyran-4-ol(tetrahydro-2H-thiopyran-4-ol) is an organic compound with the chemical formula C5H9OS. It is a colorless liquid with a special thiol odor.
tetrahydro-2H-thiopyran-4-ol have a variety of uses in organic synthesis. It can play an important role in organic synthesis as catalyst, solvent and reagent. It is often used as an intermediate in the synthesis of thioglycans, antiviral drugs, hormones and other organic compounds. In addition, it can also be used to prepare surfactants, study fluorescent dyes and protein structures.
The method for producing tetrahydro-2H-thiopyran-4-ol is usually obtained by reacting hydrogen sulfide with cyclopentane. The specific step is to react cyclopentane with a thiol base solution (such as sodium hydroxide) to form a sulfide intermediate. The sulfide intermediate is then reduced under reducing conditions, such as in the presence of hydrogen, to provide a tetrahydro-2H-thiopyran-4-ol.
Regarding the safety information of tetrahydro-2H-thiopyran-4-ol, it is an unstable compound that is irritating, and protective measures should be paid attention. Appropriate protective equipment such as gloves, goggles and face shields should be worn during use. At the same time, tetrahydro-2H-thiopyran-4-ol contact with oxygen should be avoided to avoid fire or explosion. High temperatures and open flames should be avoided during storage and handling. For further use and operation, please refer to the relevant safety data sheets and instructions and follow the correct experimental operating procedures.
tetrahydro-2H-thiopyran-4-ol have a variety of uses in organic synthesis. It can play an important role in organic synthesis as catalyst, solvent and reagent. It is often used as an intermediate in the synthesis of thioglycans, antiviral drugs, hormones and other organic compounds. In addition, it can also be used to prepare surfactants, study fluorescent dyes and protein structures.
The method for producing tetrahydro-2H-thiopyran-4-ol is usually obtained by reacting hydrogen sulfide with cyclopentane. The specific step is to react cyclopentane with a thiol base solution (such as sodium hydroxide) to form a sulfide intermediate. The sulfide intermediate is then reduced under reducing conditions, such as in the presence of hydrogen, to provide a tetrahydro-2H-thiopyran-4-ol.
Regarding the safety information of tetrahydro-2H-thiopyran-4-ol, it is an unstable compound that is irritating, and protective measures should be paid attention. Appropriate protective equipment such as gloves, goggles and face shields should be worn during use. At the same time, tetrahydro-2H-thiopyran-4-ol contact with oxygen should be avoided to avoid fire or explosion. High temperatures and open flames should be avoided during storage and handling. For further use and operation, please refer to the relevant safety data sheets and instructions and follow the correct experimental operating procedures.
Last Update：2024-04-09 21:54:55
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CAS: 29683-23-6
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