1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole

Base Information

Chemical Name:1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole
CAS No.:80200-21-1
Molecular Formula:C22H20N2O2
Molecular Weight:344.413
Hs Code.:
DSSTox Substance ID:DTXSID10603541
Wikidata:Q82500982

Synonyms:80200-21-1;1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole;SCHEMBL10785320;DTXSID10603541

Suppliers and Price of 1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole

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 1 raw suppliers

Chemical Property of 1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:344.152477885
Heavy Atom Count:26
Complexity:405

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=C(C=C1)COC2=CC=C(C=C2)OCCN3C4=CC=CC=C4C=N3

Technology Process of 1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole

There total 2 articles about 1-{2-[4-(Benzyloxy)phenoxy]ethyl}-1H-indazole 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:

: 271-44-3
benzimidazole

: 3351-59-5
2-(4-benzyloxyphenoxy)ethyl bromide

: 88670-79-5
2-<2-<4-(benzyloxy)phenoxy>ethyl>-2H-indazole

: 80200-21-1
1-<2-<4-(benzyloxy)phenoxy>ethyl>-1H-indazole

Guidance literature:: With sodium hydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) DMF, 5 min, 2.) DMF, 60 deg C, 30 min;
DOI:10.1021/jm00370a012