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2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione

Base Information
  • Chemical Name:2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione
  • CAS No.:88683-45-8
  • Molecular Formula:C15H11NO3S
  • Molecular Weight:285.323
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70512185
  • Nikkaji Number:J2.286.580C
  • Wikidata:Q82371320
2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione

Synonyms:2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione;88683-45-8;SCHEMBL16694595;DTXSID70512185;N-(p-Methoxyphenylsulfanyl)phthalimide;2-[(4-Methoxyphenyl)sulfanyl]-1H-isoindole-1,3(2H)-dione

Suppliers and Price of 2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione
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 2 raw suppliers
Chemical Property of 2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione
Chemical Property:
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:285.04596439
  • Heavy Atom Count:20
  • Complexity:369
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:COC1=CC=C(C=C1)SN2C(=O)C3=CC=CC=C3C2=O
Technology Process of 2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione

There total 3 articles about 2-((4-Methoxyphenyl)thio)isoindoline-1,3-dione 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:
1-bromo-4-methoxy-benzene; With iodine; magnesium; lithium chloride; In tetrahydrofuran; at 55 ℃; for 2.5h; Inert atmosphere; Schlenk technique;
With zinc(II) chloride; In tetrahydrofuran; at 0 - 25 ℃; for 1h; Inert atmosphere; Schlenk technique;
phthalimidesulfenyl chloride; In tetrahydrofuran; dichloromethane; at 0 - 25 ℃; for 0.833333h; Inert atmosphere; Schlenk technique;
DOI:10.1002/anie.202009699
Guidance literature:
Multi-step reaction with 3 steps
1.1: disulfur dichloride; triethylamine / tetrahydrofuran / 2 h / 0 - 20 °C / Inert atmosphere; Schlenk technique
2.1: sulfuryl dichloride; pyridine / dichloromethane / 48 h / 20 °C / Inert atmosphere; Schlenk technique
3.1: magnesium; lithium chloride; iodine / tetrahydrofuran / 2.5 h / 55 °C / Inert atmosphere; Schlenk technique
3.2: 1 h / 0 - 25 °C / Inert atmosphere; Schlenk technique
3.3: 0.83 h / 0 - 25 °C / Inert atmosphere; Schlenk technique
With pyridine; disulfur dichloride; sulfuryl dichloride; iodine; magnesium; triethylamine; lithium chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1002/anie.202009699
Guidance literature:
With tetrachloromethane; chlorine; Beim Behandeln des Reaktionsprodukts in Aether mit Kaliumphthalimid;
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