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Catalog Number:
43238
CAS Number:
20461-99-8
Ethyl 1,3-dithiolane-2-carboxylate
Purity:
≥ 97% (GC)
Synonym(s):
1,3-Dithiolane-2-carboxylic acid ethyl ester
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Product Information

Ethyl 1,3-dithiolane-2-carboxylate is a versatile compound recognized for its unique dithiolane structure, which imparts significant reactivity and stability. This compound is particularly valuable in organic synthesis, serving as an essential building block for the development of various pharmaceuticals and agrochemicals. Its ability to participate in nucleophilic substitution reactions makes it an excellent candidate for creating complex molecular architectures. Researchers have utilized Ethyl 1,3-dithiolane-2-carboxylate in the synthesis of biologically active compounds, showcasing its potential in medicinal chemistry.

Moreover, this compound's favorable solubility characteristics enhance its applicability in diverse solvents, making it suitable for various laboratory and industrial processes. Its low toxicity profile further adds to its appeal, allowing for safer handling in research environments. Ethyl 1,3-dithiolane-2-carboxylate stands out among similar compounds due to its unique functional properties, making it a preferred choice for chemists looking to innovate in synthetic methodologies.

Synonyms
1,3-Dithiolane-2-carboxylic acid ethyl ester
CAS Number
20461-99-8
Purity
≥ 97% (GC)
Molecular Formula
C6H10O2S2
Molecular Weight
178.26
MDL Number
MFCD00005411
PubChem ID
88551
Density
1.25
Appearance
Colorless to slightly yellow to sllightly orange clear liquid
Boiling Point
85 °C/0.1 mmHg
Refractive Index
n20D 1.54
Conditions
Store at RT
General Information
Synonyms
1,3-Dithiolane-2-carboxylic acid ethyl ester
CAS Number
20461-99-8
Purity
≥ 97% (GC)
Molecular Formula
C6H10O2S2
Molecular Weight
178.26
MDL Number
MFCD00005411
PubChem ID
88551
Density
1.25
Appearance
Colorless to slightly yellow to sllightly orange clear liquid
Boiling Point
85 °C/0.1 mmHg
Refractive Index
n20D 1.54
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 1,3-dithiolane-2-carboxylate is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those with dithiolane structures that exhibit biological activity.
  • Organic Synthesis: It is employed in organic chemistry for the development of complex molecules, allowing chemists to create compounds with specific functional groups efficiently.
  • Flavor and Fragrance Industry: Ethyl 1,3-dithiolane-2-carboxylate can be used in the formulation of flavors and fragrances, enhancing the sensory profile of products.
  • Polymer Chemistry: The compound is utilized in the production of specialty polymers, contributing to materials with unique properties such as improved thermal stability and flexibility.
  • Research in Material Science: It is explored for its potential applications in developing new materials, particularly in creating coatings and adhesives that require specific chemical resistance.

Citations