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2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine

Base Information Edit
  • Chemical Name:2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine
  • CAS No.:124489-20-9
  • Molecular Formula:C13H12 N4 O
  • Molecular Weight:240.264
  • Hs Code.:
  • UNII:JC2M95KK23
  • DSSTox Substance ID:DTXSID50154406
  • Nikkaji Number:J277.646D
  • Wikidata:Q83021631
  • Metabolomics Workbench ID:124301
  • ChEMBL ID:CHEMBL1743302
  • Mol file:124489-20-9.mol
2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine

Synonyms:2-hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine;2-hydroxyamino-PhIP;N-hydroxy-PHIP;N-OH-PhIP

Suppliers and Price of 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine
Supply Marketing:Edit
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
Total 3 raw suppliers
Chemical Property of 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine Edit
Chemical Property:
  • Vapor Pressure:9.98E-11mmHg at 25°C 
  • Boiling Point:497.8°Cat760mmHg 
  • Flash Point:254.8°C 
  • PSA:62.97000 
  • Density:1.35g/cm3 
  • LogP:2.50940 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:240.10111102
  • Heavy Atom Count:18
  • Complexity:282
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C2=C(N=CC(=C2)C3=CC=CC=C3)N=C1NO
  • Uses 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine is a mutagenic metablite of PhIP. PhIP is the most abundant mutagenic heterocyclic amine in cooked foods. Studies have shown the activation of 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine results in the formation of PhIP adducts and 5-OH-PhIP.
Technology Process of 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine

There total 5 articles about 2-Hydroxyamino-1-methyl-6-phenylimidazo(4,5-b)pyridine 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 hydrazine hydrate; palladium on activated charcoal; In tetrahydrofuran; at -20 - 0 ℃; for 1.5h;
DOI:10.1021/jo070306p
Guidance literature:
Multi-step reaction with 2 steps
1: 52 percent Turnov. / NaNO2; acetic acid / H2O / 3.5 h / 0 - 20 °C
2: 93 percent / hydrazine hydrate / Pd/C / tetrahydrofuran / 1.5 h / -20 - 0 °C
With hydrazine hydrate; acetic acid; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; water;
DOI:10.1021/jo070306p
Guidance literature:
Multi-step reaction with 3 steps
1: 20 percent Turnov. / 15-crown-5; NaNH2 / xylene / 1.5 h / 130 °C
2: 52 percent Turnov. / NaNO2; acetic acid / H2O / 3.5 h / 0 - 20 °C
3: 93 percent / hydrazine hydrate / Pd/C / tetrahydrofuran / 1.5 h / -20 - 0 °C
With 15-crown-5; hydrazine hydrate; sodium amide; acetic acid; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; water; xylene; 1: Chichibabin reaction;
DOI:10.1021/jo070306p
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