141367-99-9 Usage
Molecular structure
Consists of a pyrrole ring with a carboxylic acid group at the 3-position, a cyclohexyl group at the 1-position, and a 2-(2-hydroxyphenyl)-4-phenyl group at the 2-position.
Organic compound
It is an organic molecule with potential biological activities.
Functional groups
Contains a carboxylic acid group, phenyl group, hydroxyphenyl group, and cyclohexyl group.
Biological interactions
The presence of the phenyl and hydroxyphenyl groups suggest potential for interaction with biological targets.
Pharmaceutical research
It is a possible candidate for pharmaceutical and medicinal research due to its structural features.
Solubility and stability
The cyclohexyl group may contribute to its solubility and stability in various solvents, which could be important for its use in medicinal applications.
Check Digit Verification of cas no
The CAS Registry Mumber 141367-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141367-99:
(8*1)+(7*4)+(6*1)+(5*3)+(4*6)+(3*7)+(2*9)+(1*9)=129
129 % 10 = 9
So 141367-99-9 is a valid CAS Registry Number.
141367-99-9Relevant articles and documents
Tricyclic heteroaromatic systems. Synthesis of 1,3 and 1,2 disubstituted [1]benzopyrano[4,3-b]pyrrol-4-ones and structure-activity relationships as benzodiazepine receptor ligands
Colotta,Cecchi,Melani,Filacchioni,Martini,Gelli,Lucacchini
, p. 1139 - 1154 (2007/10/02)
The synthesis of some 1,3- and 1,2- disubstituted [1]benzopyrano-pyrrol-4-ones is reported as well as their benzodiazepine receptor affinity, as measured by the ability to displace [3H]flunitrazepam from its specific central binding. The struct
