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2-Azaadenine

Base Information Edit
  • Chemical Name:2-Azaadenine
  • CAS No.:2308-56-7
  • Molecular Formula:C4H4N6
  • Molecular Weight:136.116
  • Hs Code.:2933990090
  • NSC Number:57048
  • UNII:7P0OW7JL4V
  • DSSTox Substance ID:DTXSID10177651
  • Nikkaji Number:J247.709B
  • Wikidata:Q83047954
  • Mol file:2308-56-7.mol
2-Azaadenine

Synonyms:2-aza-adenine;2-azaadenine

Suppliers and Price of 2-Azaadenine
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
  • AccelPharmtech
  • 7H-Imidazo[4,5-d]-1,2,3-triazin-4-amine 97.00%
  • 25G
  • $ 8510.00
  • AccelPharmtech
  • 7H-Imidazo[4,5-d]-1,2,3-triazin-4-amine 97.00%
  • 5G
  • $ 4530.00
  • AccelPharmtech
  • 7H-Imidazo[4,5-d]-1,2,3-triazin-4-amine 97.00%
  • 1G
  • $ 2640.00
Total 2 raw suppliers
Chemical Property of 2-Azaadenine Edit
Chemical Property:
  • Vapor Pressure:0.00673mmHg at 25°C 
  • Boiling Point:270.7°Cat760mmHg 
  • Flash Point:117.5°C 
  • PSA:93.37000 
  • Density:2.26g/cm3 
  • LogP:-0.08870 
  • XLogP3:-1.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:136.04974415
  • Heavy Atom Count:10
  • Complexity:127
Purity/Quality:

99%min *data from raw suppliers

7H-Imidazo[4,5-d]-1,2,3-triazin-4-amine 97.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=NC2=NN=NC(=C2N1)N
Technology Process of 2-Azaadenine

There total 2 articles about 2-Azaadenine 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 water; sodium nitrite;

Reference yield:

Guidance literature:
NH4OH; Triazin V;
DOI:10.1007/BF00470508
Guidance literature:
at 37 ℃; for 16h; alginate gel-entrapped cells of auxotrophic thymine-dependent strain of E. coli, ammonium acetate buffer pH 5.7;
DOI:10.1135/cccc19942303
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