17106-08-0 Usage
1H-Pyrrole-2-carboxylic acid, 3,4,5-trimethyl-(9CI) properties and specific content
A chemical compound consisting of 9 carbon atoms, 11 hydrogen atoms, 1 nitrogen atom, and 2 oxygen atoms.
Derivative of pyrrole
A modified version of the parent compound pyrrole, which is a five-membered aromatic heterocycle containing one nitrogen atom.
Carboxylic acid group
A functional group (-COOH) present in the compound, contributing to its acidic properties and solubility in water.
Methyl substituents
Three methyl groups (-CH3) attached to the pyrrole ring, specifically at positions 3, 4, and 5, which influence the compound's chemical reactivity and physical properties.
Aromatic structure
The compound has an aromatic character due to the presence of the pyrrole ring, which follows the principles of aromaticity (4n+2 π electrons).
Pharmaceutical applications
The compound has potential uses in the pharmaceutical industry, as it is being studied for its biological activities and possible therapeutic effects.
Biological activities
Currently under investigation for its potential as an anti-inflammatory and antioxidant agent, which could lead to the development of new drugs for various diseases and conditions.
Interest in drug development and medicinal chemistry
The compound's chemical structure and properties make it a valuable candidate for further research in drug development and medicinal chemistry, potentially leading to new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 17106-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17106-08:
(7*1)+(6*7)+(5*1)+(4*0)+(3*6)+(2*0)+(1*8)=80
80 % 10 = 0
So 17106-08-0 is a valid CAS Registry Number.
17106-08-0Relevant articles and documents
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Jackson et al.
, p. 603 (1967)
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The Chemistry of Pyrrolic Compounds. LXI Petroporphyrins from the Julia Creek Oil Shale: Further Evidence for the Derivation of Aetiotype Petroporphyrins from Chlorophyll
Clezy, Peter S.,Fookes, Christopher J. R.,Prashar, Jognandan K.
, p. 775 - 786 (2007/10/02)
The synthesis of the porphyrins (2c-j) has been achieved by the oxidative cyclization of appropriately substituted biladienes-ac.The availability of authentic material has allowed the finalization of the structure of a series of aetiotype fossil porphyrins which vary in substitution pattern at positions 3 and 13.All combinations of H, Me and Et at these positions have now been isolated from natural sources.This points to a common precursor, possibly a divinylporphyrin, and strengthens the belief that the chlorophylls are the prime source of the petroporphyrins.A vinyl group, or a close derivative, is found at position 3 of all chlorophylls while fragmentation of the ubiquitous isocyclic ring of the chlorophylls could yield the vinyl group at position 13.
