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CAS RN: 2613-27-6 | Product Number: N0743

4-Nitrophenylsulfur Pentafluoride


Purity: >96.0%(GC)
Synonyms:
Product Documents:
1G
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5G
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Product Number N0743
Purity / Analysis Method >96.0%(GC)
Molecular Formula / Molecular Weight C__6H__4F__5NO__2S = 249.16 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
CAS RN 2613-27-6
Reaxys Registry Number 1986023
PubChem Substance ID 87559738
MDL Number

MFCD00221619

Specifications
Appearance White or Colorless to Yellow powder to lump to clear liquid
Purity(GC) min. 96.0 %
Melting point 37.0 to 41.0 °C
Properties (reference)
Melting Point 39 °C
Boiling Point 77 °C/12 mmHg
Refractive Index 1.47
Solubility in water Insoluble
GHS
Pictogram Pictogram
Signal Word Danger
Hazard Statements H301 + H311 + H331 : Toxic if swallowed, in contact with skin or if inhaled.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P261 : Avoid breathing dust.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth.
P302 + P352 + P312 : IF ON SKIN: Wash with plenty of water. Call a POISON CENTER/doctor if you feel unwell.
P403 + P233 : Store in a well-ventilated place. Keep container tightly closed.
Related Laws:
Transport Information:
UN Number UN2811
Class 6.1
Packing Group III
HS Number 2930909599
Application
4-ニトロフェニルサルファーペンタフルオリドの位置選択的アリール化反応

N0743

A 25 mL Schlenk tube equipped with a magnetic stir bar is charged with (allylPdCl)2 (2.5 mol%), PCy3·HBF4 (7.5 mol%), and K2CO3 (1.8 equiv.). The reaction tube is evacuated and bakfilled with N2 (4 times), then 2,2-dimethylbutyric acid (0.3 equiv.), bromobenzene (2.5 equiv.), toluene (1.0 mL) and 4-nitrophenylsulfur pentafluoride (0.3 mmol, 1.0 equiv.) are added subsequently. The sealed tube is screw capped and heated to 130 °C for 15h. The reaction vessel is then cooled to room temperature, and the reaction mixture is concentrated in vacuo directly. The resulting residue is purified with silica gel chromatography to afford 2'-nitro-[1,1':3',1''-terphenyl]-5'-yl sulfurpentafluoride in 87% yield.

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