Metoprine

Base Information

• Chemical Name: Metoprine
• CAS No.: 7761-45-7
• Molecular Formula: C11H10Cl2N4
• Molecular Weight: 269.133
• NSC Number: 19494,7364
• UNII: 2L9RKX796Q
• DSSTox Substance ID: DTXSID0057831
• Nikkaji Number: J9.654G
• Wikidata: Q27085870
• NCI Thesaurus Code: C1161
• Metabolomics Workbench ID: 149090
• ChEMBL ID: CHEMBL264373
• Mol file: 7761-45-7.mol

Synonyms:2,4-diamino-5-(3',4'-dichlorophenyl)-6-methylpyrimidine;BW 1970;BW 50,197;DDMP;methodichlorophen;methodichlorophen hydrochloride;metoprine

Chemical Property of Metoprine

Chemical Property:

• Vapor Pressure: 1.64E-09mmHg at 25°C
• Melting Point: 275-276oC
• Refractive Index: 1.6300 (estimate)
• Boiling Point: 483.7°C at 760 mmHg
• Flash Point: 246.3°C
• PSA: 77.82000
• Density: 1.447
• LogP: 4.08560
• Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
• Solubility.: DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated)
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 268.0282517
• Heavy Atom Count: 17
• Complexity: 266

Purity/Quality:

99% ^*data from raw suppliers

Metoprine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C(=NC(=N1)N)N)C2=CC(=C(C=C2)Cl)Cl
• Uses: A 2,4-Diaminopyrimidine derivative as antimalarial agent.

Technology Process of Metoprine

There total 1 articles about Metoprine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ metoprine (7761-45-7)

Guidance literature:

/BRN= 192580/;

DOI:10.1021/ja01152a060