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Catalog Number:
43264
CAS Number:
20462-00-4
Ethyl 1,3-dithiane-2-carboxylate
Purity:
≥ 98% (GC)
Synonym(s):
1,3-Dithiane-2-carboxylic acid ethyl ester
Hazmat
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Product Information

Ethyl 1,3-dithiane-2-carboxylate is a versatile compound known for its unique structure and functional properties, making it a valuable asset in various chemical applications. This compound features a dithiane ring, which enhances its reactivity and stability, allowing it to serve as an effective building block in organic synthesis. Researchers and industry professionals often utilize Ethyl 1,3-dithiane-2-carboxylate in the development of pharmaceuticals, agrochemicals, and specialty chemicals due to its ability to facilitate complex reactions and improve yields. Its distinct properties enable the synthesis of diverse derivatives, which can be tailored for specific applications, thus expanding its utility in research and industrial processes.

In addition to its role in organic synthesis, Ethyl 1,3-dithiane-2-carboxylate is recognized for its potential in the production of fine chemicals and intermediates. Its favorable reactivity profile allows for efficient transformations, making it an attractive choice for chemists seeking to optimize their synthetic routes. The compound's stability and ease of handling further enhance its appeal, ensuring that it meets the rigorous demands of both laboratory and industrial environments. With its broad range of applications and benefits, Ethyl 1,3-dithiane-2-carboxylate stands out as a key ingredient for innovative chemical solutions.

Synonyms
1,3-Dithiane-2-carboxylic acid ethyl ester
CAS Number
20462-00-4
Purity
≥ 98% (GC)
Molecular Formula
C7H12O2S2
Molecular Weight
192.29
MDL Number
MFCD00006657
PubChem ID
88552
Density
1.22
Appearance
Colorless to slightly yellow to sllightly orange clear liquid
Boiling Point
75 - 77 °C
Refractive Index
n20D 1.54
Conditions
Store at RT
General Information
Synonyms
1,3-Dithiane-2-carboxylic acid ethyl ester
CAS Number
20462-00-4
Purity
≥ 98% (GC)
Molecular Formula
C7H12O2S2
Molecular Weight
192.29
MDL Number
MFCD00006657
PubChem ID
88552
Density
1.22
Appearance
Colorless to slightly yellow to sllightly orange clear liquid
Boiling Point
75 - 77 °C
Refractive Index
n20D 1.54
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Synthetic Organic Chemistry: This compound serves as a versatile building block in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Pharmaceutical Development: It is used in the design of new pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects, enhancing drug discovery processes.
  • Agricultural Chemistry: The compound finds applications in developing agrochemicals, such as pesticides and herbicides, contributing to more effective crop protection solutions.
  • Material Science: Ethyl 1,3-dithiane-2-carboxylate is utilized in the production of specialty polymers and materials, offering unique properties that improve product performance.
  • Analytical Chemistry: It acts as a reagent in various analytical techniques, aiding in the identification and quantification of other chemical substances in research and quality control laboratories.

Citations