2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran

Base Information

Chemical Name:2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran
CAS No.:122823-57-8
Molecular Formula:C15H14OTe
Molecular Weight:337.876
Hs Code.:
DSSTox Substance ID:DTXSID10577410
Nikkaji Number:J1.012.305D

Synonyms:MAO-B-IN-29;122823-57-8;2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran;DTXSID10577410;HY-157517;CS-0955488

Suppliers and Price of 2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran

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
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price

Total 1 raw suppliers

Chemical Property of 2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:340.0106878
Heavy Atom Count:17
Complexity:237

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(OC2=CC=CC=C21)C[Te]C3=CC=CC=C3

Technology Process of 2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran

There total 6 articles about 2-[(Phenyltellanyl)methyl]-2,3-dihydro-1-benzofuran 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: 96.0%

: 39652-06-7
benzenetellurinyl acetate

: 1745-81-9
o-Allylphenol

: 122823-57-8
2,3-dihydro-2-<(phenyltelluro)methyl>benzofuran

Guidance literature:: With tin(IV) chloride; In chloroform; for 0.5h; Ambient temperature; var. Lewis acids, other temp., var. times;
DOI:10.1021/jo00279a030