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5-Acetyl-2-methoxybenzenesulfonyl chloride

Base Information
  • Chemical Name:5-Acetyl-2-methoxybenzenesulfonyl chloride
  • CAS No.:85276-41-1
  • Molecular Formula:C9H9ClO4S
  • Molecular Weight:248.687
  • Hs Code.:2914700090
  • DSSTox Substance ID:DTXSID30406137
  • Wikidata:Q82211031
  • Mol file:85276-41-1.mol
5-Acetyl-2-methoxybenzenesulfonyl chloride

Synonyms:85276-41-1;5-acetyl-2-methoxybenzenesulfonyl chloride;5-acetyl-2-methoxybenzene-1-sulfonyl chloride;BENZENESULFONYL CHLORIDE, 5-ACETYL-2-METHOXY-;DTXSID30406137;AKOS002662789;CS-0248447;EN300-399151

Suppliers and Price of 5-Acetyl-2-methoxybenzenesulfonyl chloride
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
  • American Custom Chemicals Corporation
  • 5-ACETYL-2-METHOXY-BENZENESULFONYL CHLORIDE 95.00%
  • 5MG
  • $ 497.24
  • AK Scientific
  • 5-Acetyl-2-methoxybenzenesulfonylchloride
  • 1g
  • $ 676.00
Total 4 raw suppliers
Chemical Property of 5-Acetyl-2-methoxybenzenesulfonyl chloride
Chemical Property:
  • PSA:68.82000 
  • LogP:2.90610 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:247.9910076
  • Heavy Atom Count:15
  • Complexity:333
Purity/Quality:

99% *data from raw suppliers

5-ACETYL-2-METHOXY-BENZENESULFONYL CHLORIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)C1=CC(=C(C=C1)OC)S(=O)(=O)Cl
Technology Process of 5-Acetyl-2-methoxybenzenesulfonyl chloride

There total 3 articles about 5-Acetyl-2-methoxybenzenesulfonyl chloride 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 chlorosulfonic acid; thionyl chloride; at 20 ℃; for 26h;
DOI:10.1016/j.ejmech.2019.05.013
Guidance literature:
With hydrogenchloride; sulfur dioxide; sodium nitrite; Yield given. Multistep reaction; 1.) AcOH, 5 deg C, 30 min 2.) AcOH, 0-5 deg C;
DOI:10.1248/cpb.30.4092
Guidance literature:
Multi-step reaction with 2 steps
1.1: iron; ammonium chloride / water; ethanol / 50 - 80 °C
2.1: hydrogenchloride; acetic acid; sodium nitrite / water / -10 - -5 °C
2.2: 10 °C
With hydrogenchloride; iron; ammonium chloride; acetic acid; sodium nitrite; In ethanol; water;
DOI:10.1021/jm501504k
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