1,2,3-Benzotriazin-4-amine

Base Information

Chemical Name:1,2,3-Benzotriazin-4-amine
CAS No.:89795-80-2
Molecular Formula:C₇H₆N₄
Molecular Weight:146.151
Hs Code.:2933699090
DSSTox Substance ID:DTXSID30340229
Wikidata:Q82109760
Mol file:89795-80-2.mol

Synonyms:89795-80-2;1,2,3-Benzotriazin-4-amine;4-aminoazacinnoline;1,2,3-Benzotriazin-4-amine(9CI);SCHEMBL133576;4-Aminobenzo-1,2,3-triazine;DTXSID30340229;1,2,3-Benzotriazin-4-amine #;AKOS006315414

Suppliers and Price of 1,2,3-Benzotriazin-4-amine

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

Total 4 raw suppliers

Chemical Property of 1,2,3-Benzotriazin-4-amine

Chemical Property:

PSA：64.69000
LogP:1.18820
XLogP3:0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:146.059246208
Heavy Atom Count:11
Complexity:138

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=NN=N2)N

Technology Process of 1,2,3-Benzotriazin-4-amine

There total 9 articles about 1,2,3-Benzotriazin-4-amine 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: 33.0%

: 408322-05-4
1,3-diaminoindazole

: 89795-80-2
4-aminobenzo-1,2,3-triazine

Guidance literature:: With chloroform; at 20 ℃; for 720h;
DOI:10.1023/A:1011600420626

Reference yield: 24.0%

: 1-amino-3-azidoindazole

: 89795-80-2
4-aminobenzo-1,2,3-triazine

Guidance literature:: With chloroform; at 20 ℃; for 648h;
DOI:10.1023/A:1011600420626

Reference yield:

: 185011-16-9
1-amino-3-nitroindazole

: 89795-80-2
4-aminobenzo-1,2,3-triazine

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 2 percent Pd/C / methanol / 8 h / 40 - 45 °C

2: 33 percent / CHCl₃ / 720 h / 20 °C

With chloroform; hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1023/A:1011600420626