5-(4-chlorophenyl)furan-2-carbaldehyde

5-(4-chlorophenyl)furan-2-carbaldehyde

(E)-3-(5-nitrofuran-2-yl)acrylaldehyde

(E)-3-(5-nitrofuran-2-yl)acrylaldehyde

(R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione

$250.00
CAS No.: 490-83-5
Catalog No.: 194454
Purity: 95%
MF: C6H6O6
MW: 174.108
Storage: 2-8 degree Celsius
SMILES: O[C@@H](CO)[C@@H]1C(C(C(O1)=O)=O)=O
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194454
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(R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione; CAS No.: 490-83-5; (R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione. PROPERTIES: (R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione is a crystalline solid. Its molecular formula is C6H6O5, and the molecular weight is approximately 154.11 g/mol. The compound has a melting point of approximately 180-182 C. It is slightly soluble in water but dissolves well in organic solvents such as methanol and ethyl acetate. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a furan ring and multiple hydroxyl groups, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, (R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione serves as a versatile intermediate. The hydroxyl groups can undergo reactions such as etherification and esterification. The furan ring provides unique electronic effects. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antiviral drugs, the structure of (R)-5-((S)-1,2-dihydroxyethyl)furan-2,3,4(5H)-trione can be modified to enhance the drug's antiviral activity and pharmacokinetic properties (as described in medicinal chemistry research articles). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as mentioned in organic chemistry research papers).

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