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2-(Fluorosulfonyl)difluoroacetic acid

Basic information Safety Supplier Related

2-(Fluorosulfonyl)difluoroacetic acid Basic information

Product Name:
2-(Fluorosulfonyl)difluoroacetic acid
Synonyms:
  • 2-(FLUOROSULFONYL)DIFLUOROACETIC ACID
  • 2-(FLUOROSULPHONYL)DIFLUOROACETIC ACID
  • 2,2-DIFLUORO-2-(FLUOROSULFONYL)ACETATE
  • 2,2-DIFLUORO-2-(FLUOROSULFONYL)ACETIC ACID
  • 2,2-Difluoro-2-(fluorosulfony)acetic Acid
  • 2,2-Difluoro-2-(fluorosulphonyl)ethanoic acid
  • Difluoro(fluorosulphonyl)acetic acid
  • 2,2-Difluoro-2-(fluorosulfonyl)acetic acid, 94%, 97%
CAS:
1717-59-5
MF:
C2HF3O4S
MW:
178.09
EINECS:
808-179-4
Product Categories:
  • Miscellaneous Reagents, Sulfur & Selenium Compounds
  • Sulfonyl Halides
  • Difluoromethylation
  • Sulfonyl Fluorides
  • Sulfur Compounds
  • Synthetic Reagents
  • Alkyl Fluorinated Building Blocks
  • Building Blocks
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Fluorination Reagents
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Sulfonyl Halides
  • Organic Building Blocks
  • Sulfur Compounds
  • bc0001
Mol File:
1717-59-5.mol
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2-(Fluorosulfonyl)difluoroacetic acid Chemical Properties

Boiling point:
153 °C(lit.)
Density 
1.723 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.36(lit.)
Flash point:
>230 °F
solubility 
Chloroform (Soluble), DMSO (Slightly)
form 
liquid
pka
-0.38±0.10(Predicted)
color 
colorless
Water Solubility 
It is soluble in water.
Sensitive 
Moisture Sensitive
CAS DataBase Reference
1717-59-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,T+
Risk Statements 
34-35-27/28
Safety Statements 
26-27-36/37/39-45-28
RIDADR 
UN 1760 8/PG 2
WGK Germany 
3
Hazard Note 
Corrosive
TSCA 
No
HazardClass 
8
PackingGroup 
II
HS Code 
29159000

MSDS

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2-(Fluorosulfonyl)difluoroacetic acid Usage And Synthesis

Uses

Difluorocarbene source for the difluoromethylation of alcohols.

Uses

2,2-Difluoro-2-(fluorosulfonyl)acetic acid, is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as an important reagent in the synthesis of difluorocarbenes and difluorocyclopropanes.

Uses

An important reagent in the synthesis of difluorocarbenes and difluorocyclopropanes.

General Description

2,2-Difluoro-2-(fluorosulfonyl)acetic acid reagent is employed as a difluorocarbene source for difluoromethylation of phenolic hydroxyl groups.

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