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1-(5-amino-2-fluorophenyl)pyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

926215-19-2

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926215-19-2 Usage

Type of Compound

Pyrrolidinone derivative

Functional Groups

Amino group and fluorophenyl group

Usage

Pharmaceutical research and drug development

Potential Therapeutic Properties

Treatment for neurological disorders, anticonvulsant, anti-inflammatory, and analgesic properties

Structure

The compound consists of a pyrrolidinone ring fused to a phenyl ring, with an amino group at the 5-position of the phenyl ring and a fluorine atom at the 2-position.

Significance

AFP's structure and properties make it a promising candidate for further investigation in the development of new pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 926215-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,2,1 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 926215-19:
(8*9)+(7*2)+(6*6)+(5*2)+(4*1)+(3*5)+(2*1)+(1*9)=162
162 % 10 = 2
So 926215-19-2 is a valid CAS Registry Number.

926215-19-2Relevant articles and documents

Heterocyclically Substituted Anilinopyrimides

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, (2011/10/13)

Heterocyclically substituted anilinopyrimidines of the formula (I) in which R1 to R10 and L1, L2, E1, E2, E3, Y and Z have the meanings given in the description, and agrochemically active salts thereof, their use and also methods and compositions for controlling phytopathogenic harmful fungi in and/or on plants or in and/or on seed of plants, processes for preparing such compositions and treated seed and also their use for controlling phytopathogenic harmful fungi in agriculture, horticulture and forestry, in the protection of materials and in the domestic and hygiene field. The present invention furthermore relates to a process for preparing heterocyclically substituted anilinopyrimidinenes of the formula (I).

NOVEL POTASSIUM CHANNEL BLOCKERS

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Page/Page column 36-37, (2010/04/06)

The present invention provides a compound of formula (I) or its salts or pharmaceutically acceptable derivatives thereof wherein; X1 is selected from a group consisting of CH, O or N; R1 is selected from the group consisting of optionally substituted arylalkyl, and optionally substituted heteroarylalkyl; R2 is selected from the group consisting of optionally substituted aryl, optionally substituted heteroaryl or NR6R7; R3 is selected from the group consisting of hydrogen, halogen, hydroxyl, alkoxy, aryloxy, optionally substituted alkyl, optionally substituted amino, optionally substituted amino sulphonyl or nitrile; R4 is selected from the group consisting of optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted acyl, optionally substituted sulfonyl, optionally substituted sulfamoyl, optionally substituted aryl, optionally substituted arylalkyl, and optionally substituted heteroaryl R5 may be hydrogen or may, together with R4 and X1 (when X1= N), form an optionally substituted saturated or partially saturated 5-7 membered ring with the general formula (II). X2 is C(=O), C(R8)2; X3 is, C(R9)2, N(R9b), O or S; R6 and R7 are the same or different and each represents hydrogen, optioanally substituted alkyl, optionally substituted cycloalkyl, optionally substituted arylalkyl, optionally substituted aryl or optionally substituted heteroaryl; R8a and R8bfor each occurence is independently hydrogen, halogen, optionally substituted amino, optionally substituted amino carbonyl, hydroxyl, optionally substituted acyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted arylalky, optionally substituted aryl or optionally substituted heteroaryl; R9a R9b for each occurence is independently hydrogen, halogen, optionally substituted amino, optionally substituted amino carbonyl, hydroxyl, optionally substituted acyl, optionally substituted alkoxy, optionally substituted aryloxy, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted arylalky, optionally substituted aryl or optionally substituted heteroaryl; R9c is optionally substituted acyl, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted arylalky, optionally substituted aryl or optionally substituted heteroaryl; With the proviso that: When X1 is O then j = 0 When X1 is N or CH then j =1 n = 1,2 or 3. The compounds are useful as potassium ion channel inhibitors.

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