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CAS 1003-04-9 Food Grade Tetrahydrothiophen-3-One Thiophene Chemical 99% High Purity

Place of Origin China
Brand Name hoyoshee
Certification ISO9001
Model Number HYS-049
Minimum Order Quantity Negotiable
Price Negotiable
Packaging Details 25kg/ Drum
Delivery Time 5-8 working days
Payment Terms L/C,D/A,D/P,T/T,Western Union,MoneyGram
Supply Ability 100 Ton/Month

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Product Details
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.)
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CAS 1003-04-9 thiophene compound

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High Purity Tetrahydrothiophen-3-one

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Food Grade Tetrahydrothiophen-3-one

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Product Description
High Purity Food Grade Tetrahydrothiophen-3-one
Product Description
CAS 1003-04-9 Food Grade Tetrahydrothiophen-3-One Thiophene Chemical 99% High Purity 0

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
Primary Functions and Uses

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).

1. Primary Function: Key Synthetic Intermediate

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.
2. Primary Uses by Industry
A. Pharmaceutical Industry

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.
B. Agrochemical Industry

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.