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2(1H)-Pyridinone, 4-hydroxy-3,6-dimethylis an organic compound with the molecular formula C7H7NO2. It is a derivative of pyridinone, featuring a hydroxyl group at the 4-position, and two methyl groups at the 3 and 6 positions. 2(1H)-Pyridinone, 4-hydroxy-3,6-dimethylis known for its potential applications in the pharmaceutical and chemical industries due to its unique structural properties.

4664-13-5

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4664-13-5 Usage

Uses

Used in Pharmaceutical Industry:
2(1H)-Pyridinone, 4-hydroxy-3,6-dimethylis used as a reactant for the preparation of pyridine and pyrimidine derivatives. These derivatives have potential applications as ACTH (adrenocorticotropic hormone) releasing factor antagonists. ACTH releasing factor antagonists are important in the treatment of various conditions related to the endocrine system, such as Cushing's disease and Nelson's syndrome.

Check Digit Verification of cas no

The CAS Registry Mumber 4664-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4664-13:
(6*4)+(5*6)+(4*6)+(3*4)+(2*1)+(1*3)=95
95 % 10 = 5
So 4664-13-5 is a valid CAS Registry Number.

4664-13-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3,6-dimethyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 2,4-dihydroxy-3,6-dimethylpyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4664-13-5 SDS

4664-13-5Relevant academic research and scientific papers

Minimizing the contribution of enterohepatic recirculation to clearance in rat for the NCINI class of inhibitors of HIV

Fader, Lee D.,Carson, Rebekah,Morin, Sébastien,Bilodeau, Fran?ois,Chabot, Catherine,Halmos, Ted,Bailey, Murray D.,Kawai, Stephen H.,Coulombe, René,Laplante, Steven,Mekhssian, Kevork,Jakalian, Araz,Garneau, Michel,Duan, Jianmin,Mason, Stephen W.,Simoneau, Bruno,Fenwick, Craig,Tsantrizos, Youla,Yoakim, Christiane

supporting information, p. 711 - 716 (2014/07/07)

A scaffold replacement approach was used to identifying the pyridine series of noncatalytic site integrase inhibitors. These molecules bind with higher affinity to a tetrameric form compared to a dimeric form of integrase. Optimization of the C6 and C4 po

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

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Page/Page column 45, (2010/12/01)

Compounds of formula I wherein a, R1, R2, R3, R4, R5 and R6 are defined herein, are useful as inhibitors of HIV replication.

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