635313-72-3 Usage
Derivative of pyrrole
A modified version of the pyrrole molecule, which is a five-membered aromatic ring containing one nitrogen atom.
Carboxylic acid group
A functional group (-COOH) attached to the pyrrole ring, contributing to the compound's acidic properties.
Hydroxyethyl side chain
A side chain (-CH2CH2OH) attached to the 5 position of the pyrrole ring, which may influence the compound's solubility and reactivity.
5 position substitution
The location of the hydroxyethyl side chain on the pyrrole ring, which can affect the compound's chemical properties and reactivity.
Potential applications in pharmaceuticals and drug development
The unique structure and properties of 1H-Pyrrole-2-carboxylic acid, 5-(1-hydroxyethyl)(9CI) may make it useful in the creation of new drugs and therapies.
Biological activities
The compound may exhibit interactions with biological systems, which could be explored for potential therapeutic applications.
Building block in the synthesis of organic compounds
The compound can be used as a starting material or intermediate in the synthesis of other organic molecules, potentially leading to new chemical products.
Need for further research and studies
More investigation is required to fully understand the specific uses and potential benefits of 1H-Pyrrole-2-carboxylic acid, 5-(1-hydroxyethyl)(9CI) in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 635313-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,3,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 635313-72:
(8*6)+(7*3)+(6*5)+(5*3)+(4*1)+(3*3)+(2*7)+(1*2)=143
143 % 10 = 3
So 635313-72-3 is a valid CAS Registry Number.
635313-72-3Relevant articles and documents
Ring-deactivated hydroxyalkylpyrrole-based inhibitors of α-chymotrypsin: Synthesis and mechanism of action
Martyn, Derek C.,Vernall, Andrea J.,Clark, Bruce M.,Abell, Andrew D.
, p. 2103 - 2110 (2007/10/03)
13C NMR and mass spectrometry studies have been used to demonstrate that the inhibition of α-chymotrypsin by N-sulfonylhydroxymethylpyrrole inhibitors (10) is non-covalent. Hydroxyalkylpyrroles in which an electron-withdrawing group (acyl substituent) is introduced at the alternative C2 position have been synthesised and also shown to inactivate α-chymotrypsin. SAR studies on this class suggests that the incorporation of phenylalanine at C2 is favoured, however, there is little gain in introducing a hydrophobic substituent at C5.
