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Catalog Number:
29785
CAS Number:
1003-04-9
4,5-Dihydro-3(2 H -thiophénone
Purity:
≥ 99% (GC)
Synonym(s):
3-Thiophanone, Tétrahydrothiophène-3-one
Hazmat
Documents
$22.03 /25G
Taille
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Product Information

Utilisé pour mélanger des boissons gazeuses, des boissons, des produits à base de viande, des confiseries et des arômes de produits laitiers.

Synonyms
3-Thiophanone, Tétrahydrothiophène-3-one
CAS Number
1003-04-9
Purity
≥ 99% (GC)
Molecular Formula
C6H6OS
Molecular Weight
102.15
MDL Number
MFCD00005412
PubChem ID
61252
Density
1,194 g/mL à 25 °C
Appearance
Liquide incolore à jaune clair
Boiling Point
175 °C
Refractive Index
n20/D 1,528
General Information
Synonyms
3-Thiophanone, Tétrahydrothiophène-3-one
CAS Number
1003-04-9
Purity
≥ 99% (GC)
Molecular Formula
C6H6OS
Molecular Weight
102.15
MDL Number
MFCD00005412
PubChem ID
61252
Density
1,194 g/mL à 25 °C
Appearance
Liquide incolore à jaune clair
Boiling Point
175 °C
Refractive Index
n20/D 1,528
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4,5-Dihydro-3(2H)-thiophenone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in creating novel analgesics and anti-inflammatory agents.
  • Flavor and Fragrance Industry: Its unique odor profile makes it valuable in formulating flavors and fragrances, providing a distinct aroma that enhances consumer products.
  • Material Science: Employed in the development of specialty polymers and coatings, it contributes to materials with improved durability and resistance to environmental factors.
  • Agricultural Chemistry: The compound is explored for its potential in creating agrochemicals, including pesticides and herbicides, offering safer alternatives for crop protection.
  • Research Applications: It is used in academic and industrial laboratories for various chemical reactions, helping researchers understand reaction mechanisms and develop new synthetic pathways.

Citations