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Technology Process of 2-Sulfoanthraquinone sodium salt

2-Sulfoanthraquinone sodium salt

Base Information
  • Chemical Name:2-Sulfoanthraquinone sodium salt
  • CAS No.:131-08-8
  • Molecular Formula:C14H8 O5 S . Na
  • Molecular Weight:310.262
  • Hs Code.:29147090
  • NSC Number:215188,4757
  • Wikidata:Q7553294
  • Mol file:131-08-8.mol
2-Sulfoanthraquinone sodium salt

Synonyms:Silver salt;2-Anthraquinonesulfonate sodium;Sodium 2-anthrachinonesulfonate;2-Anthraquinone sodium sulfonate;2-Sulfoanthraquinone sodium salt;9,10-Anthraquinone-2-sodium sulfonate;Sodium .beta.-anthraquinonesulfonate;WLN: L C666 BV IVJ ESWQ &-NA-;NSC-215188;1-Anthracenesulfonic acid,10-dihydro-9,10-dioxo-, sodium salt;2-Anthracenesulfonic acid,10-dihydro-9,10-dioxo-, sodium salt;NSC4757;NSC-4757;NSC215188;LS-20387;Q7553294

Suppliers and Price of 2-Sulfoanthraquinone sodium salt
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
  • Sigma-Aldrich
  • Sodium anthraquinone-2-sulfonate ≥98% (HPLC)
  • 50g
  • $ 48.20
  • Sigma-Aldrich
  • Sodium anthraquinone-2-sulfonate ≥98% (HPLC)
  • 500g
  • $ 286.00
  • Crysdot
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 95+%
  • 100g
  • $ 50.00
  • BLDpharm
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98+%
  • 500g
  • $ 58.00
  • BLDpharm
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98+%
  • 25g
  • $ 7.00
  • BLDpharm
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98+%
  • 100g
  • $ 15.00
  • Arctom
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98%
  • 100g
  • $ 25.00
  • Arctom
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98%
  • 25g
  • $ 10.00
  • Arctom
  • Sodium9,10-dioxo-9,10-dihydroanthracene-2-sulfonate 98%
  • 500g
  • $ 89.00
  • American Custom Chemicals Corporation
  • ANTHRAQUINONE-2-SULFONIC ACID SODIUM SALT 95.00%
  • 500G
  • $ 4467.29
Total 97 raw suppliers
Chemical Property of 2-Sulfoanthraquinone sodium salt
Chemical Property:
  • Appearance/Colour:beige powder 
  • Vapor Pressure:0Pa at 25℃ 
  • Melting Point:>300 ºC 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA：99.72000 
  • Density:g/cm3 
  • LogP:2.44690 
  • Storage Temp.:Store below +30°C. 
  • Water Solubility.:Soluble in hot water, cold water and insoluble in alcohol or ether. 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:310.99901381
  • Heavy Atom Count:21
  • Complexity:532
Purity/Quality:

98.5% *data from raw suppliers

Sodium anthraquinone-2-sulfonate ≥98% (HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)S(=O)(=O)O.[Na+]
Refernces

Palladium-Catalyzed Aerobic Oxidative Dehydrogenation of Cyclohexenes to Substituted Arene Derivatives

10.1021/ja512770u

The research explores a palladium(II)-catalyzed aerobic oxidative dehydrogenation method for converting substituted cyclohexenes into arene derivatives. The study aims to develop an efficient and sustainable route for synthesizing aromatic compounds, which are crucial in various industrial applications, including pharmaceuticals. The researchers identified that using sodium anthraquinone-2-sulfonate (AMS) as a cocatalyst significantly enhanced product yields. The method demonstrated good tolerance for a wide range of functional groups and provided an alternative to traditional synthetic methods that often rely on stoichiometric oxidants like DDQ and Mn oxides. The study concluded that this catalytic dehydrogenation process offers a more convergent and environmentally friendly approach to synthesizing substituted aromatics, as illustrated by its application in the preparation of a phthalimide-based TRPA1 activity modulator, showcasing potential use in the synthesis of biologically active compounds.

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