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460365-08-6

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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.

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