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2-Methylpyrido[3,4-d]pyrimidin-4-ol is a heterocyclic chemical compound with the molecular formula C10H8N2O. It is a derivative of pyridine and pyrimidine, featuring a methyl group attached to the second carbon atom of the pyridine ring. The presence of the hydroxyl group (OH) in its structure endows it with potential for drug development and medicinal chemistry research. Its unique structural features and possible biological activities make 2-Methylpyrido[3,4-d]pyrimidin-4-ol a compound of interest for further study and potential therapeutic applications.

22389-85-1

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22389-85-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Methylpyrido[3,4-d]pyrimidin-4-ol is used as a potential pharmaceutical candidate for drug development due to its heterocyclic nature and the presence of a hydroxyl group, which can facilitate interactions with biological targets and contribute to its therapeutic effects.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Methylpyrido[3,4-d]pyrimidin-4-ol is utilized as a compound of interest for studying its potential biological activities and exploring its applications in the design of new drugs. Its structural features make it a valuable starting point for the synthesis of novel compounds with improved pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 22389-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22389-85:
(7*2)+(6*2)+(5*3)+(4*8)+(3*9)+(2*8)+(1*5)=121
121 % 10 = 1
So 22389-85-1 is a valid CAS Registry Number.

22389-85-1SDS

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 2-methyl-1H-pyrido[3,4-d]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:22389-85-1 SDS

22389-85-1Relevant academic research and scientific papers

Pyrido[3,4-d]pyrimidin-4(3H)-one metabolism mediated by aldehyde oxidase is blocked by C2-substitution

Hayes, Angela,Mok, N. Yi,Liu, Manjuan,Thai, Ching,Henley, Alan T.,Atrash, Butrus,Lanigan, Rachel M.,Sejberg, Jemmy,Le Bihan, Yann-Va?,Bavetsias, Vassilios,Blagg, Julian,Raynaud, Florence I.

, p. 771 - 777 (2017)

1.We have previously described C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-one derivatives as cell permeable inhibitors of the KDM4 and KDM5 subfamilies of JmjC histone lysine demethylases. 2.Although exemplar compound 1 exhibited moderate clearance in mo

Preparation and Structure-Activity Relationships of 4-Substituted Amino-2-methylpyridopyrimidines as Cytokinin Analogs

Nishikawa, Shiro,Nishikimi, Yoshio,Maki, Shinji,Kumazawa, Zenzaburo,Kashimura, Naoki

, p. 1034 - 1038 (2007/10/02)

Various 4-substituted amino derivatives of 2-methylpyridopyrimidine were prepared to investigate their structure-cytokinin activity relationships.Both an Amaranthus betacyanin and a lettuce seed germination bioassay revealed that most anilino and s

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