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5-Nitro-2-phenylsulfonylmethylbenzaldehyde

Base Information
  • Chemical Name:5-Nitro-2-phenylsulfonylmethylbenzaldehyde
  • CAS No.:155534-53-5
  • Molecular Formula:C14H11NO5S
  • Molecular Weight:305.311
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40447430
  • Nikkaji Number:J2.142.698I
  • Wikidata:Q82266300
  • Mol file:155534-53-5.mol
5-Nitro-2-phenylsulfonylmethylbenzaldehyde

Synonyms:5-nitro-2-phenylsulfonylmethylbenzaldehyde;155534-53-5;SCHEMBL4176109;DTXSID40447430;OWQJSRUZDKLDPT-UHFFFAOYSA-N;5-nitro-2-phenylsufonylmethylbenzaldehyde;2-(Phenylsulfonylmethyl)-5-nitrobenzaldehyde

Suppliers and Price of 5-Nitro-2-phenylsulfonylmethylbenzaldehyde
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 5-Nitro-2-phenylsulfonylmethylbenzaldehyde
Chemical Property:
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:305.03579362
  • Heavy Atom Count:21
  • Complexity:473
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)S(=O)(=O)CC2=C(C=C(C=C2)[N+](=O)[O-])C=O
Technology Process of 5-Nitro-2-phenylsulfonylmethylbenzaldehyde

There total 6 articles about 5-Nitro-2-phenylsulfonylmethylbenzaldehyde 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 Dess-Martin periodane; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1039/c9ob01745c
Guidance literature:
Multi-step reaction with 3 steps
1: 98 percent / p-TsOH / toluene / Heating
2: 35 percent / KOH; DMSO / 23 °C
3: aq. AcOH / 5 h / Heating
With potassium hydroxide; toluene-4-sulfonic acid; acetic acid; dimethyl sulfoxide; In toluene;
DOI:10.1021/ja0449168
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