90490-64-5 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(4-methoxyphenyl)-2-(1H-pyrrol-1-yl)is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its versatile functional groups allow for multiple reaction pathways, facilitating the synthesis of a wide range of compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethanone, 1-(4-methoxyphenyl)-2-(1H-pyrrol-1-yl)is employed as a building block for the development of new pharmaceutical agents. Its unique structure may contribute to the discovery of novel drugs with specific therapeutic targets and properties.
Used in Drug Discovery and Development:
Ethanone, 1-(4-methoxyphenyl)-2-(1H-pyrrol-1-yl)plays a significant role in drug discovery and development, where it may serve as a precursor or a template for designing new molecules with potential medicinal applications. Its presence in various chemical libraries aids researchers in identifying promising candidates for further investigation.
Used in the Production of Fine Chemicals and Pharmaceuticals:
This chemical compound is also used in the manufacturing process of fine chemicals and pharmaceuticals, where its unique properties can enhance the quality, efficacy, or stability of the final products.
Further research and studies are essential to fully explore the properties and potential applications of Ethanone, 1-(4-methoxyphenyl)-2-(1H-pyrrol-1-yl)-, ensuring its optimal utilization in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 90490-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,9 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90490-64:
(7*9)+(6*0)+(5*4)+(4*9)+(3*0)+(2*6)+(1*4)=135
135 % 10 = 5
So 90490-64-5 is a valid CAS Registry Number.
90490-64-5Relevant academic research and scientific papers
Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Acyclic α- N-Pyrrolyl/Indolyl Ketones
Alexy, Eric J.,Lavernhe, Remi,Stoltz, Brian M.,Zhang, Haiming
supporting information, (2020/06/05)
The synthesis of fully substituted α-N-pyrrolyl and indolyl ketones via enantioselective palladium-catalyzed allylic alkylation is described. The acyclic ketones are alkylated in high yields with high enantioselectivities through the use of an electron-deficient phosphinooxazoline ligand, furnishing a highly congested and synthetically challenging stereocenter. The obtained alkylation products contain multiple reactive sites poised for additional functionalizations and diversification.
