720011

Potassium 2-iodo-5-methylbenzenesulfonate

• Sinónimos: Pre-IBS
• Fórmula empírica (notación de Hill): C₇H₆IKO₃S
• Número de CAS: 1093215-92-9
• Peso molecular: 336.19
• MDL number: MFCD12031330
• UNSPSC Code: 12352101
• PubChem Substance ID: 329763691
• NACRES: NA.22

Propiedades

• form: powder
• Quality Level: 100
• reaction suitability: reagent type: oxidant
• greener alternative product characteristics: Catalysis; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• mp: 288-292 °C
• functional group: iodo; sulfonic acid
• greener alternative category: Aligned,
• storage temp.: 2-8°C
• SMILES string: [K+].Cc1ccc(I)c(c1)S([O-])(=O)=O
• InChI: 1S/C7H7IO3S.K/c1-5-2-3-6(8)7(4-5)12(9,10)11;/h2-4H,1H3,(H,9,10,11);/q;+1/p-1
• InChI key: LFQHEPUFDZVNHD-UHFFFAOYSA-M

Descripción

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Find details here.

Application

• Catalyst for alcohol oxidation

Catalyst for greener oxidation of alcohols using Oxone as the terminal oxidant. Alternative to stoichiometric hypervalent iodine oxidants.

2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone

Other Notes

Strategies for generating peptide radical cations via ion/ion reactions.


Gas phase click chemistry via ion/ion reactions.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H302,H315,H319,H335
• pcodes: P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable