IMidazo[1,2-b]pyridazine-3,6-diaMine

Base Information

Chemical Name:IMidazo[1,2-b]pyridazine-3,6-diaMine
CAS No.:166176-50-7
Molecular Formula:C6H7N5
Molecular Weight:149.15328
Hs Code.:2933990090
Mol file:166176-50-7.mol

Synonyms:IMidazo[1,2-b]pyridazine-3,6-diaMine

Suppliers and Price of IMidazo[1,2-b]pyridazine-3,6-diaMine

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

Crysdot
Imidazo[1,2-b]pyridazine-3,6-diamine 95+%
1g
$ 880.00

Alichem
Imidazo[1,2-b]pyridazine-3,6-diamine
1g
$ 778.26

AccelPharmtech
Imidazo[1,2-b]pyridazine-3,6-diamine 97.00%
5G
$ 2960.00

Total 3 raw suppliers

Chemical Property of IMidazo[1,2-b]pyridazine-3,6-diaMine

Chemical Property:

PSA：82.96000
LogP:0.40500

Purity/Quality:

≥99% ^*data from raw suppliers

Imidazo[1,2-b]pyridazine-3,6-diamine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of IMidazo[1,2-b]pyridazine-3,6-diaMine

There total 2 articles about IMidazo[1,2-b]pyridazine-3,6-diaMine 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: 74.0%

: 37990-33-3
6-amino-3-nitroimidazo[1,2-b]pyridazine

: 166176-50-7
3,6-diaminoimidazo[1,2-b]pyridazine

Guidance literature:: With hydrogen; nickel; In tetrahydrofuran; at 20 ℃; for 2.5h;
DOI:10.7164/antibiotics.53.1071

Reference yield:

: 18087-76-8
6-chloro-3-nitroimidazo<1,2-b>pyridazine

: 166176-50-7
3,6-diaminoimidazo[1,2-b]pyridazine

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / aq. NH₃ / tetrahydrofuran / 7 h / 120 °C

2: 74 percent / H₂ / Raney Ni / tetrahydrofuran / 2.5 h / 20 °C

With ammonium hydroxide; hydrogen; nickel; In tetrahydrofuran;
DOI:10.7164/antibiotics.53.1071