19813-55-9 Usage
Uses
Used in Organic Synthesis:
METHYL 3-HYDROXY-5-METHOXY-2-THIOPHENECARBOXYLATE is used as a key intermediate in the synthesis of complex organic compounds, facilitating the creation of a diverse range of chemical entities with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, METHYL 3-HYDROXY-5-METHOXY-2-THIOPHENECARBOXYLATE is used as a building block for the preparation of biologically active molecules, contributing to the development of new drugs with therapeutic potential.
Used in Medicinal Chemistry:
METHYL 3-HYDROXY-5-METHOXY-2-THIOPHENECARBOXYLATE is employed for its antioxidant and anti-inflammatory effects, making it a valuable compound in the advancement of treatments for various diseases and conditions.
Used in Drug Development:
Due to its pharmacological properties, METHYL 3-HYDROXY-5-METHOXY-2-THIOPHENECARBOXYLATE is utilized in the development of new drugs, potentially offering novel therapeutic options for unmet medical needs.
Check Digit Verification of cas no
The CAS Registry Mumber 19813-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19813-55:
(7*1)+(6*9)+(5*8)+(4*1)+(3*3)+(2*5)+(1*5)=129
129 % 10 = 9
So 19813-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O4S/c1-10-5-3-4(8)6(12-5)7(9)11-2/h3,8H,1-2H3
19813-55-9Relevant academic research and scientific papers
Reactions with Methyl 3-Hydroxythiophene-2-carboxylate. Part 2. A New Route to Mono- and Di-alkyl Ethers of Thiotetronic and α-Halogenothiotetronic Acids
Corral, Carlos,Lissavetzky, Jaime
, p. 2711 - 2714 (2007/10/02)
Methyl 2-chloro-3-oxo-2,3-dihydrothiophene-2-carboxylates (2), obtained from methyl 3-hydroxythiophene-2-carboxylate by straightforward halogenation, added alcohols and then lost hydrogen chloride at room temperature to yield thiophene-2,4-diols (4).Succe
