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CAS RN: 1868173-15-2 | Product Number: T3622

[(4-Trifluoromethyl)phenyl](2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate


Purity: >95.0%(HPLC)(qNMR)
Synonyms:
  • [(4-Trifluoromethyl)phenyl](2,4,6-trimethoxyphenyl)iodonium Tosylate
Product Documents:
200MG
$78.00
1   1   5  
1G
$236.00
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Supplemental Product Information:

This product is commercialized in partnership with Dr. Stuart and PSU.

Product Number T3622
Purity / Analysis Method >95.0%(HPLC)(qNMR)
Molecular Formula / Molecular Weight C__2__3H__2__2F__3IO__6S = 610.38 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Condition to Avoid Light Sensitive,Heat Sensitive
CAS RN 1868173-15-2
Reaxys Registry Number 29449543
PubChem Substance ID 354334572
Specifications
Appearance White to Light yellow powder to crystal
Purity(HPLC) min. 95.0 %(excluding counter anion)
Purity(qNMR) min. 95.0 %
NMR confirm to structure
Properties (reference)
Melting Point 171 °C(dec.)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P302 + P352 : IF ON SKIN: Wash with plenty of soap and water.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
P362 : Take off contaminated clothing and wash before reuse.
Related Laws:
Transport Information:
HS Number 2930.90.2900
Application
Asymmetric Diaryliodonium Tosylates Useful for Metal-free Arylations

P2412,T3622,D5145,B5269,T1110,F1111, B5573

References


Application
Hypervalent iodine compounds usable for arylating reactions

Stuart et al. have designed and synthesized some diaryl-substituted hypervalent iodine compounds having a 1,3,5-trimethoxybenzene (TMB) moiety and an aromatic ring. In these compounds, the TMB moiety acts as a leaving group so that the other aromatic ring can be used for the aryl group introduction. Various functional groups such as cyano, nitro, fluoro, or chloro substituted aromatic TMB hypervalent iodine compounds have been reported so far. It is expected to use these compounds for transition-metal-free arylations.

References


PubMed Literature


Articles/Brochures

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