4-Phenoxypyridin-3-amine

Base Information

Chemical Name:4-Phenoxypyridin-3-amine
CAS No.:132038-28-9
Molecular Formula:C₁₁H₁₀N₂O
Molecular Weight:186.213
Hs Code.:
European Community (EC) Number:865-569-7

Synonyms:4-phenoxypyridin-3-amine;132038-28-9;4-Phenoxypyridin-3-ylamine;4-Phenoxy-3-pyridinamine;SCHEMBL9853825;KJZZCHNYRGOHIP-UHFFFAOYSA-N;AKOS009233602;CS-0252698;EN300-61298;Z359373618

Suppliers and Price of 4-Phenoxypyridin-3-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 2 raw suppliers

Chemical Property of 4-Phenoxypyridin-3-amine

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:186.079312947
Heavy Atom Count:14
Complexity:169

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC2=C(C=NC=C2)N

Technology Process of 4-Phenoxypyridin-3-amine

There total 6 articles about 4-Phenoxypyridin-3-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: 92.0%

: 132038-21-2
3-nitro-4-phenoxypyridine

: 132038-28-9
4-phenoxy-3-pyridinamine

Guidance literature:: With hydrogenchloride; tin(ll) chloride; In methanol; water; at 80 ℃;
DOI:10.1016/j.bmcl.2009.08.051

Reference yield:

: 5435-54-1
4-hydroxy-3-nitropyridine

: 132038-28-9
4-phenoxy-3-pyridinamine

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / toluene / 110 °C

2: potassium carbonate / N,N-dimethyl-formamide / 80 °C

3: tin(II) chloride dihdyrate; hydrogenchloride / methanol / 80 °C

With hydrogenchloride; tin(II) chloride dihdyrate; potassium carbonate; trichlorophosphate; In methanol; N,N-dimethyl-formamide; toluene;
DOI:10.1039/c4tc01791a

Reference yield:

: 13091-23-1
4-chloro-3-nitropyridine

: 132038-28-9
4-phenoxy-3-pyridinamine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 80 °C

2: tin(II) chloride dihdyrate; hydrogenchloride / methanol / 80 °C

With hydrogenchloride; tin(II) chloride dihdyrate; potassium carbonate; In methanol; N,N-dimethyl-formamide;
DOI:10.1039/c4tc01791a