112919-61-6 Usage
Molecular structure
1H-Pyrrole-2-carboxylic acid, 1-[2,6-bis(1-methylethyl)phenyl]-, methyl ester is a heterocyclic compound consisting of a pyrrole ring with a carboxylic acid group at position 2, a phenyl group at position 1, and a methyl ester group attached to the carboxylic acid.
Biological activity
The compound has potential biological activities, including anti-inflammatory and anti-cancer effects, due to the presence of the 2-carboxylic acid and phenyl groups in its structure.
Solubility and bioavailability
The addition of the methyl ester group to the compound increases its solubility and bioavailability, making it more easily absorbed and utilized by the body.
Medicinal use
The increased solubility and bioavailability of the compound make it potentially useful for medicinal purposes, although further research is needed to determine its exact pharmacological profile and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 112919-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112919-61:
(8*1)+(7*1)+(6*2)+(5*9)+(4*1)+(3*9)+(2*6)+(1*1)=116
116 % 10 = 6
So 112919-61-6 is a valid CAS Registry Number.
112919-61-6Relevant articles and documents
The Synthesis of Methyl 1-Aryl-2-pyrrolecarboxylates
Kiely, John S.,Huang, Suchin
, p. 1137 - 1139 (2007/10/02)
A series of alkyl 1-(aryl)-2-pyrrolecarboxylates were prepared by the condensation of the appropriate aniline with methyl tetrahydro-2,5-dimethoxy-2-furancarboxylate in refluxing acetic acid.It was found that condensation proceeds even in substituents possessing steric bulk are present in the ortho positions of the aniline.Strong electron withdrawing substituents if conjugated to the nitrogen diverts the reaction from product to unidentified tars.
