2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide

Base Information

Chemical Name:2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide
CAS No.:61395-30-0
Molecular Formula:Br*C₁₅H₁₂NO₃
Molecular Weight:334.169
Hs Code.:
DSSTox Substance ID:DTXSID50493428

Synonyms:61395-30-0;SCHEMBL11765998;DTXSID50493428;BHBKUYKKSIEALE-UHFFFAOYSA-M;2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide;2-(2-Acetyloxyphenyl)Isoxazolo[2,3-a]Pyridinium Bromide

Suppliers and Price of 2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:333.00006
Heavy Atom Count:20
Complexity:333

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1=CC=CC=C1C2=CC3=CC=CC=[N+]3O2.[Br-]

Technology Process of 2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide

There total 3 articles about 2-[2-(Acetyloxy)phenyl][1,2]oxazolo[2,3-a]pyridin-8-ium bromide 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: 73.0%

: 61395-30-0
2-(2-acetoxy-phenyl)-isoxazolo[2,3-a]pyridinylium; bromide

Guidance literature:

Reference yield:

: 61395-08-2
1-(2-hydroxy-phenyl)-2-(1-oxy-pyridin-2-yl)-ethanone

: 61395-30-0
2-(2-acetoxy-phenyl)-isoxazolo[2,3-a]pyridinylium; bromide

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HBr / acetic acid / 5 h / Heating

2: 1.5 h / Heating

With hydrogen bromide; In acetic acid;
DOI:10.1021/jo00428a021