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1-Methyl-1H-perimidine

Base Information
  • Chemical Name:1-Methyl-1H-perimidine
  • CAS No.:19585-93-4
  • Molecular Formula:C12H10 N2
  • Molecular Weight:182.22
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID00173248
  • Nikkaji Number:J49.985D
  • Wikidata:Q83043319
  • ChEMBL ID:CHEMBL1725173
  • Mol file:19585-93-4.mol
1-Methyl-1H-perimidine

Synonyms:1-Methyl-1H-perimidine;1-Methylperimidine;Perimidine, 1-methyl-;19585-93-4;1H-Perimidine, 1-methyl-;BRN 0880273;1H-Perimidine, 1-methyl- (9CI);5-23-08-00213 (Beilstein Handbook Reference);MLS001196768;SCHEMBL5849197;CHEMBL1725173;DTXSID00173248;HMS2873J03;AKOS006273097;NCGC00245863-01;SMR000555851;LS-102424;EU-0076846

Suppliers and Price of 1-Methyl-1H-perimidine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 1-METHYL-1H-PERIMIDINE 95.00%
  • 5MG
  • $ 500.72
Total 3 raw suppliers
Chemical Property of 1-Methyl-1H-perimidine
Chemical Property:
  • Vapor Pressure:1.9E-05mmHg at 25°C 
  • Boiling Point:362.7°Cat760mmHg 
  • Flash Point:173.2°C 
  • PSA:17.82000 
  • Density:1.17g/cm3 
  • LogP:2.72650 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:182.084398327
  • Heavy Atom Count:14
  • Complexity:249
Purity/Quality:

99% *data from raw suppliers

1-METHYL-1H-PERIMIDINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C=NC2=CC=CC3=C2C1=CC=C3
  • General Description 1H-Perimidine, 1-methyl- (9CI), also known as 1-Methylperimidine, is a tricyclic heterocyclic compound that exhibits structural and tautomeric properties, as evidenced by NMR studies. It serves as a key scaffold in the synthesis of derivatives like 2-cyano- and 2-carbamoylperimidines, which are accessible through nucleophilic substitution reactions. Additionally, perimidine derivatives, including those with methyl substitution, have been explored for their potential as DNA-intercalating agents due to their planar tricyclic structure, which facilitates binding to DNA with moderate affinity and cytotoxic activity, though they lack in vivo efficacy.
Technology Process of 1-Methyl-1H-perimidine

There total 10 articles about 1-Methyl-1H-perimidine 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:
Guidance literature:
With potassium hydroxide; In dimethyl sulfoxide; for 2h; Ambient temperature;
Guidance literature:
With sodium disulfite; In ethanol; water; for 1.5h; Heating;
DOI:10.1007/BF00475399
Guidance literature:
With potassium hydroxide; In ethanol; for 3h; Ambient temperature;
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