Bis(2-methoxyethyl)aminosulfur trifluoride

Bis(2-methoxyethyl)aminosulfur trifluoride
  • CAS No.:202289-38-1
Other grades of this product :

Bis(2-methoxyethyl)aminosulfur trifluoride Basic information
Product Name:Bis(2-methoxyethyl)aminosulfur trifluoride
Synonyms:DEOXO-FLUOR(R);BIS(2-METHOXYETHYL)AMINO-SULFUR TRIFLUORIDE;BIS(2-METHOXYETHYL)AMINOSULPHUR TRIFLUORIDE;BAST  Deoxo-Fluor ,Bis(2-methoxyethyl)aminosulfur trifluoride;2-methoxy-N-(2-methoxyethyl)-N-(trifluoro-λ4-sulfanyl)ethanamine;Bis(6-methoxyethyl)aminosulfur trifluoride;bis(2-methoxyethyl)(trifluoro-λ-sulfanyl)amine;Deoxo-Fluor (Air Prods. Chem.)
CAS:202289-38-1
MF:C6H14F3NO2S
MW:221.24
EINECS:478-190-3
Product Categories:Fluorinating Reagents;Nucleophilic Fluorinating Reagents;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Synthetic Organic Chemistry
Mol File:202289-38-1.mol
Bis(2-methoxyethyl)aminosulfur trifluoride Chemical Properties
Boiling point >80°C
density 1.2 g/mL at 25 °C(lit.)
refractive index 1.4270 to 1.4310
Fp 205 °F
storage temp. 2-8°C
form liquid
pka-7.46±0.70(Predicted)
color clear yellow
Specific Gravity1.2
Merck 14,2897
InChIKeyAPOYTRAZFJURPB-UHFFFAOYSA-N
CAS DataBase Reference202289-38-1(CAS DataBase Reference)
EPA Substance Registry SystemSulfur, trifluoro[2-methoxy-N-(2-methoxyethyl)ethanaminato-.kappa.N]-, (T-4)- (202289-38-1)
Safety Information
Hazard Codes T,C,F
Risk Statements 14-23/25-29-35-67-65-63-48/20-25-11-40-37-19
Safety Statements 23-26-36/37/39-43-45-8-62-46-25-16
RIDADR UN REST
WGK Germany 3
10-21
Hazard Note Toxic/Corrosive
HazardClass KEEP COLD, CORROSIVE
PackingGroup 
HS Code 29319090
MSDS Information
ProviderLanguage
SigmaAldrichEnglish
ACROSEnglish
Bis(2-methoxyethyl)aminosulfur trifluoride Usage And Synthesis
Chemical PropertiesDark yellow-orange liquid
UsesVersatile, thermally stable nucleophilic fluorinating reagent.
UsesReactant for:
  • Fluorination reactions

  • Preparation of fluorinated catechols via Umpolung based nucleophilic deoxyfluorination

  • Preparation of imidazole derivatives as CXCR3 antagonists

  • Ring expansion reactions

  • Synthesis of acyl azides from carboxylic acids

  • Aldehydes or ketones from carboxylic acids and Grignard reagents via in situ generation of Weinreb amides

Bis(2-methoxyethyl)aminosulfur trifluoride Preparation Products And Raw materials

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