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1,6-dihydro-4-hydroxy-2-methyl-6-oxonicotinonitrile is a chemical compound with the molecular formula C7H9N3O2. It is a derivative of nicotinic acid and features a six-membered ring with a hydroxyl group, a nitrile group, and a methyl group attached to the second carbon. This white to beige solid is soluble in water and other polar solvents, and is primarily utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

64169-92-2

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64169-92-2 Usage

Uses

Used in Pharmaceutical Synthesis:
1,6-dihydro-4-hydroxy-2-methyl-6-oxonicotinonitrile serves as an intermediate in the production of various drugs, contributing to the development of new medications for different therapeutic areas.
Used in Agrochemical Production:
In agricultural applications, 1,6-dihydro-4-hydroxy-2-methyl-6-oxonicotinonitrile has demonstrated potential as an antifungal agent, helping to protect crops from fungal infections and diseases.
Used in Bioactive Molecule Preparation:
1,6-dihydro-4-hydroxy-2-methyl-6-oxonicotinonitrile also acts as a building block in the preparation of bioactive molecules, which can have various applications in the fields of medicine and biology, including the development of new pharmaceutical agents and the study of biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 64169-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,6 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64169-92:
(7*6)+(6*4)+(5*1)+(4*6)+(3*9)+(2*9)+(1*2)=142
142 % 10 = 2
So 64169-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O2/c1-4-5(3-8)6(10)2-7(11)9-4/h2H,1H3,(H2,9,10,11)

64169-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-2-methyl-6-oxo-1H-pyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Pyridinecarbonitrile,1,6-dihydro-4-hydroxy-2-methyl-6-oxo

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:64169-92-2 SDS

64169-92-2Relevant academic research and scientific papers

INDAZOLES AND AZAINDAZOLES AS LRRK2 INHIBITORS

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Page/Page column 408; 409, (2021/01/29)

The present invention is directed to indazole and azaindazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS disorders.

SUBSTITUTED BICYCLE HETEROCYCLIC DERIVATIVES USEFUL AS ROMK CHANNEL INHIBITORS

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Page/Page column 152; 153, (2018/06/06)

Disclosed are compounds of Formula (I) or a salt thereof, wherein R1 is (II) or (III); each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, Rd, R3, L1, L2, R1a, R1b, R1c, and n are define herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.

NOVEL COMPOUNDS THAT ARE ERK INHIBITORS

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Page/Page column 146, (2014/04/17)

Disclosed are the ERK inhibitors of formula (1): and the pharmaceutically acceptable salts thereof. Also disclosed are methods of treating cancer using the compounds of formula (1).

Synthesis and biological evaluation of C-5 methyl substituted 4-arylthio and 4-aryloxy-3-iodopyridin-2(1H)-one type anti-HIV agents

Guillemont, Jér?me,Benjahad, Abdellah,Oumouch, Said,Decrane, Laurence,Palandjian, Patrice,Vernier, Daniel,Queguiner, Laurence,Andries, Koen,De Béthune, Marie-Pierre,Hertogs, Kurt,Grierson, David S.,Nguyen, Chi Hung

scheme or table, p. 7473 - 7487 (2010/06/11)

A series of C-5 methyl substituted 4-arylthio- and 4-aryloxy-3-iodopyridin- 2(1H)-ones has been synthesized as new pyridinone analogues for their evaluation as anti-HIV inhibitors. The optimization at the 5-position was developed through an efficient use of the key intermediates 5-ethoxycarbonyl- and 5-cyano-pyridin-2(1H)-ones (14 and 15). Biological studies revealed that several compounds show potent HIV-1 reverse transcriptase inhibitory properties, for example, compounds 93 and 99 are active at 0.6-50 nM against wild type HIV-1 and a panel of major simple/double HIV mutant strains.

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