1247706-41-7 Usage
Structure
Oxazole ring with a carboxylic acid group and a chlorophenyl group The oxazole ring is the central core of the molecule, with a chlorine-containing phenyl group and a carboxylic acid group attached to it.
Application
Pharmaceutical industry 2-(2-chlorophenyl)oxazole-4-carboxylic acid is commonly used in the synthesis of potential drugs and as a building block for various organic reactions in the pharmaceutical industry.
Chlorophenyl group
Structural diversity The presence of the chlorophenyl group contributes to the structural diversity of the compound, which can be useful for drug development.
Oxazole ring
Biological activities The oxazole ring has been found to exhibit various biological activities, making it an important component of the compound.
Importance
Medicinal chemistry and drug discovery The unique structure and potential pharmacological properties of 2-(2-chlorophenyl)oxazole-4-carboxylic acid make it an important chemical in the fields of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 1247706-41-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,7,7,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1247706-41:
(9*1)+(8*2)+(7*4)+(6*7)+(5*7)+(4*0)+(3*6)+(2*4)+(1*1)=157
157 % 10 = 7
So 1247706-41-7 is a valid CAS Registry Number.
1247706-41-7Relevant academic research and scientific papers
Synthesis and bioactivity of phenyl substituted furan and oxazole carboxylic acid derivatives as potential PDE4 inhibitors
Lin, Yinuo,Ahmed, Wasim,He, Min,Xiang, Xuwen,Tang, Riyuan,Cui, Zi-Ning
, (2020/10/02)
In this present study, a series of 5-phenyl-2-furan and 4-phenyl-2-oxazole derivatives were designed and synthesized as phosphodiesterase type 4 (PDE4) inhibitors. In vitro results showed that the synthesized compounds exhibited considerable inhibitory ac
Hydroxamic Acids as Potent Inhibitors of FeII and MnII E. coli Methionine Aminopeptidase: Biological Activities and X-ray Structures of Oxazole Hydroxamate-EcMetAP-Mn Complexes
Huguet, Florian,Melet, Armelle,Alves de Sousa, Rodolphe,Lieutaud, Aurelie,Chevalier, Jacqueline,Maigre, Laure,Deschamps, Patrick,Tomas, Alain,Leulliot, Nicolas,Pages, Jean-Marie,Artaud, Isabelle
, p. 1020 - 1030 (2012/07/31)
New series of acids and hydroxamic acids linked to five-membered heterocycles including furan, oxazole, 1,2,4- or 1,3,4-oxadiazole, and imidazole were synthesized and tested as inhibitors against the FeII, CoII, and MnII f
