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2-METHOXYPHENYL-(2-THIENYL)METHANOL

Base Information Edit
  • Chemical Name:2-METHOXYPHENYL-(2-THIENYL)METHANOL
  • CAS No.:356554-06-8
  • Molecular Formula:C12H12O2S
  • Molecular Weight:220.292
  • Hs Code.:
  • Mol file:356554-06-8.mol
2-METHOXYPHENYL-(2-THIENYL)METHANOL

Synonyms:

Suppliers and Price of 2-METHOXYPHENYL-(2-THIENYL)METHANOL
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of 2-METHOXYPHENYL-(2-THIENYL)METHANOL Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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Technology Process of 2-METHOXYPHENYL-(2-THIENYL)METHANOL

There total 6 articles about 2-METHOXYPHENYL-(2-THIENYL)METHANOL 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:
Guidance literature:
thiophene boronic acid; With diethylzinc; In toluene; at 70 ℃; for 6h; Inert atmosphere;
With (S,E)-2-(anthracen-9-ylmethyleneamino)-4-methyl-1,1-diphenylpentan-1-ol; In toluene; at 20 ℃; for 0.5h; Inert atmosphere;
ortho-anisaldehyde; In toluene; at 0 - 20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1016/j.tetasy.2009.02.059
Guidance literature:
With 1,10-Phenanthroline; 3-chloroprop-1-ene; trifluoroacetic acid; cobalt(II) bromide; zinc; In acetonitrile; at 80 ℃; for 16h; Inert atmosphere; Sealed tube;
DOI:10.1002/chem.201806239
Guidance literature:
With potassium fluoride; rhodium(III) chloride; bromo[N,N'-bis[(Rp)-(+)-12-methoxy-4-[2.2]paracyclophanyl]imidazol-2-ylidene]silver; In methanol; tert-butyl alcohol; at 40 ℃; for 3h; Overall yield = 81 %; enantioselective reaction; Sonication; Inert atmosphere;
DOI:10.1016/j.tetasy.2013.01.017
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