112799-30-1 Usage
Pyrrole derivative
A chemical compound based on the pyrrole ring structure
PDC is derived from the pyrrole structure, which is a five-membered aromatic ring containing one nitrogen atom.
Carboxylic acid group
Presence of -COOH functional group
The carboxylic acid group is an important functional group in PDC, contributing to its chemical reactivity and potential pharmaceutical properties.
Phenylthio substituent
Presence of a phenyl ring with a sulfur atom (-SPh) attached
The phenylthio group is a significant part of PDC's structure, affecting its chemical properties and potential applications.
Antimycobacterial potential
Investigated for its ability to combat mycobacterial infections
PDC has been studied for its potential as an antimycobacterial agent, which could make it useful in the development of new treatments for mycobacterial infections, such as tuberculosis.
Precursor in synthesis
Used as a starting compound for the synthesis of various biologically active compounds
Due to its unique structure and properties, PDC can serve as a precursor in the synthesis of other biologically active compounds, making it valuable in the development of new drugs and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 112799-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,9 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112799-30:
(8*1)+(7*1)+(6*2)+(5*7)+(4*9)+(3*9)+(2*3)+(1*0)=131
131 % 10 = 1
So 112799-30-1 is a valid CAS Registry Number.
112799-30-1Relevant academic research and scientific papers
4-(Phenylthio)-pyrrole-3-carboxylic Acid Esters
Eiden, Fritz,Grusdt, Ulrike
, p. 1020 - 1031 (2007/10/02)
Dihydro(dimethoxy)methylfurancarboxylic acid esters 4A/4B have been applied to the synthesis of the title compounds.With amines as catalysts they react with thiophenols to give the addition products 12a-d, which upon heating with acids eliminate methanol to form the furancarboxylic acid esters 13a-b and 17, whereas reactions with ammonia or amines lead to the pyrrolecarboxylic acid esters 20a-e.Reactions of 4 with 2-aminothiophenol yield the fused pyrrole and pyrrolidine derivatives 15 and 16.Compounds 20b and e were transformed to the benzothiopyranopyrrole carboxylic acid esters 23a and b.
