124307-91-1 Usage
Molecular structure
1H-Pyrrole-2-carboxylic acid, 5-[(acetyloxy)methyl]-3-methyl-, phenylmethyl ester is a tricyclic compound consisting of a pyrrole ring, an ester group, and an acetyloxymethyl group.
Functional groups
The compound contains a carboxylic acid group (-COOH), an ester group (-OCOCH3), an acetyloxymethyl group (-CH2C(O)OCH3), and a methyl group (-CH3).
Positional attachment
The acetyloxymethyl group is attached to the 5-position of the pyrrole ring, the phenylmethyl group is attached to the carboxylic acid, and the methyl group is at the 3-position.
Derivative of pyrrole carboxylic acid
The compound is a derivative of 1H-pyrrole-2-carboxylic acid, which means it has been modified by adding functional groups to the parent compound.
Biological activity
1H-Pyrrole-2-carboxylic acid, 5-[(acetyloxy)methyl]-3-methyl-, phenylmethyl ester has potential biological activities, making it a valuable compound in medicinal chemistry research and drug development.
Applications in pharmaceuticals
The compound may have applications in the synthesis of pharmaceuticals and as a scaffold for drug design due to its unique structure and potential biological activities.
Need for further research
More research is needed to fully understand the properties and potential uses of 1H-Pyrrole-2-carboxylic acid, 5-[(acetyloxy)methyl]-3-methyl-, phenylmethyl ester in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 124307-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124307-91:
(8*1)+(7*2)+(6*4)+(5*3)+(4*0)+(3*7)+(2*9)+(1*1)=101
101 % 10 = 1
So 124307-91-1 is a valid CAS Registry Number.
124307-91-1Relevant academic research and scientific papers
Conjugated macrocycles related to the porphyrins. 25. Proton NMR spectroscopic evidence for a preferred [18]annulene substructure in carbaporphyrins from the magnitude of selected 4JH,H CH=C-CH3 coupling constants
Liu, Dachun,Lash, Timothy D.
, p. 1755 - 1761 (2007/10/03)
Two new benzocarbaporphyrins with four or five alkyl substituents have been synthesized by the "3 + 1" MacDonald methodology. At lower temperatures, the proton NMR spectrum of the asymmetrically substituted carbaporphyrin 8 gave two NH resonances, while c
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.
