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Methyl 4-(benzo[b]thiophen-2-yl)benzoate

Base Information
  • Chemical Name:Methyl 4-(benzo[b]thiophen-2-yl)benzoate
  • CAS No.:132932-63-9
  • Molecular Formula:C16H12O2S
  • Molecular Weight:268.336
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501294237
Methyl 4-(benzo[b]thiophen-2-yl)benzoate

Synonyms:132932-63-9;Methyl 4-(benzo[b]thiophen-2-yl)benzoate;SCHEMBL732990;JDCUPUFNNLIUHS-UHFFFAOYSA-N;DTXSID501294237;Methyl 4-benzo[b]thien-2-ylbenzoate

Suppliers and Price of Methyl 4-(benzo[b]thiophen-2-yl)benzoate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Methyl 4-(benzo[b]thiophen-2-yl)benzoate
Chemical Property:
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:268.05580079
  • Heavy Atom Count:19
  • Complexity:323
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC(=O)C1=CC=C(C=C1)C2=CC3=CC=CC=C3S2
Technology Process of Methyl 4-(benzo[b]thiophen-2-yl)benzoate

There total 9 articles about Methyl 4-(benzo[b]thiophen-2-yl)benzoate 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:
With AuOH(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene); acetic acid; In toluene; at 100 ℃; for 20h;
DOI:10.1039/c8ob02196a
Guidance literature:
With 1,1,1,3',3',3'-hexafluoro-propanol; sodium acetate; palladium diacetate; silver(l) oxide; at 50 ℃; for 16h; regioselective reaction;
DOI:10.1021/jacs.8b05361
Guidance literature:
With tris(bipyridine)ruthenium(II) dichloride hexahydrate; In acetonitrile; at 25 ℃; for 12h; regioselective reaction; Inert atmosphere; Irradiation; Schlenk technique;
DOI:10.1055/s-0032-1318155
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