2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide

Base Information

Chemical Name:2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide
CAS No.:712325-30-9
Molecular Formula:C₁₇H₁₃BrN₂O₂
Molecular Weight:357.206
Hs Code.:
European Community (EC) Number:804-210-0
Wikidata:Q27089192
Pharos Ligand ID:T6GFBGBBGQBA
ChEMBL ID:CHEMBL1418045

Synonyms:VU0405601

Suppliers and Price of 2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide

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

TRC
VU0405601
10mg
$ 305.00

Sigma-Aldrich
VU0405601 ≥98% (HPLC)
25mg
$ 356.00

Sigma-Aldrich
VU0405601 ≥98% (HPLC)
5mg
$ 90.30

Matrix Scientific
2-(1-Bromonaphthalen-2-yloxy)-N-(pyridin-3-yl)acetamide 95%
5g
$ 4218.00

Matrix Scientific
2-(1-Bromonaphthalen-2-yloxy)-N-(pyridin-3-yl)acetamide 95%
1g
$ 2220.00

Total 2 raw suppliers

Chemical Property of 2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:356.01604
Heavy Atom Count:22
Complexity:380

Purity/Quality:

95%-98% ^*data from raw suppliers

VU0405601 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC(=C2Br)OCC(=O)NC3=CN=CC=C3
Uses VU0405601 is a novel selective hERG blocker.

Technology Process of 2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide

There total 1 articles about 2-(1-bromonaphthalen-2-yl)oxy-N-pyridin-3-ylacetamide 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%

: 462-08-8
pyridin-3-ylamine

: 41791-59-7
2-((1-bromonaphthalen-2-yl)oxy)acetic acid

: 712325-30-9
2-[(1-bromonaphthalen-2-yl)oxy]-N-(pyridin-3-yl)acetamide

Guidance literature:: With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.ejmech.2015.10.032