460365-08-6 Usage
Explanation
This is the full IUPAC name of the compound, which describes its structure and composition.
Explanation
This is a shorter, more commonly used name for the compound, which is derived from its structure as an ester derivative of 4-cyanophenylalanine.
Explanation
The compound is an ester derivative, which means it is formed by the reaction of an alcohol (in this case, 1,1-dimethylethyl alcohol) with a carboxylic acid (1(2H)-Pyridinecarboxylic acid).
Explanation
The compound is derived from the non-proteogenic amino acid 4-cyanophenylalanine, which is a modified version of the naturally occurring amino acid phenylalanine.
Explanation
The compound is used in various industries, particularly in the production of pharmaceuticals and as a reagent in chemical synthesis. It also has potential applications in drug development, particularly in the fields of neuropharmacology (study of drugs that affect the nervous system) and oncology (study of cancer).
Explanation
The compound's unique chemical structure allows it to have potential applications in various medicinal and research fields, making it a valuable compound for further study and development.
Explanation
The compound contains an ester functional group (formed by the reaction of an alcohol and a carboxylic acid), a cyano group (C≡N), and an aromatic ring (part of the phenyl group). These functional groups contribute to the compound's properties and potential applications.
Type of Compound
Ester derivative
Parent Amino Acid
4-Cyanophenylalanine
Applications
Pharmaceutical production, chemical synthesis, drug development, neuropharmacology, oncology
Unique Chemical Structure
Potential for medicinal and research purposes
Functional Groups
Ester, cyano, and aromatic ring
Check Digit Verification of cas no
The CAS Registry Mumber 460365-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,3,6 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 460365-08:
(8*4)+(7*6)+(6*0)+(5*3)+(4*6)+(3*5)+(2*0)+(1*8)=136
136 % 10 = 6
So 460365-08-6 is a valid CAS Registry Number.
460365-08-6Relevant articles and documents
Imidazopyridine-based fatty acid synthase inhibitors that show anti-HCV activity and in vivo target modulation
Oslob, Johan D.,Johnson, Russell J.,Cai, Haiying,Feng, Shirley Q.,Hu, Lily,Kosaka, Yuko,Lai, Julie,Sivaraja, Mohanram,Tep, Samnang,Yang, Hanbiao,Zaharia, Cristiana A.,Evanchik, Marc J.,McDowell, Robert S.
, p. 113 - 117 (2013/02/26)
Potent imidazopyridine-based inhibitors of fatty acid synthase (FASN) are described. The compounds are shown to have antiviral (HCV replicon) activities that track with their biochemical activities. The most potent analogue (compound 19) also inhibits rat FASN and inhibits de novo palmitate synthesis in vitro (cell-based) as well as in vivo.
ARYL CARBOXAMIDE DERIVATIVES AS SODIUM CHANNEL INHIBITORS FOR TREATMENT OF PAIN
-
Page/Page column 77, (2011/09/19)
The present invention provides compounds that are inhibitors of voltage-gated sodium channels (Nav), in particular Nav 1.7, and are therefore useful for the treatment of diseases treatable by inhibition of these channels, in particular, chronic pain disorders. Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.
Synthesis of 4-substituted tetrahydropyridines by cross-coupling of enol phosphates
Larsen, Uffe S.,Martiny, Lars,Begtrup, Mikael
, p. 4261 - 4263 (2007/10/03)
Enol phosphates, synthesized from 4-piperidone, react by palladium catalyzed cross-coupling with arylboronic acids and by iron and palladium catalyzed cross-coupling with Grignard reagents to give 4-substituted tetrahydropyridines.