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Potassium (E)-propenyl-1-trifluoroborate

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Potassium (E)-propenyl-1-trifluoroborate Basic information

Product Name:
Potassium (E)-propenyl-1-trifluoroborate
Synonyms:
  • PotassiuM (E)-1-propenyl-1-trifluoroborate
  • PotassiuM (E)-trifluoro(prop-1-en-1-yl)borate
  • potassiuM (E)-trifluoro(prop-1-enyl)borate
  • Potassium trans-1-propenyltrifluoroborate
  • (e)-propenyl-1-trifluoroborate
  • Potassium trifluoro(prop-1-en-1-yl)borate
  • potassium trifluoro(prop-1-en-1-yl)boranuide
  • trifluoro-[(E)-prop-1-enyl]boranuide
CAS:
804565-39-7
MF:
C3H5BF3K
MW:
147.9763096
Product Categories:
  • Organic boronic acid
  • orgnaic boroinic acid
Mol File:
804565-39-7.mol
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Potassium (E)-propenyl-1-trifluoroborate Chemical Properties

Melting point:
81-85°C
InChIKey
RLDWVFWDURMTAV-SQQVDAMQSA-N
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-39
WGK Germany 
3
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Potassium (E)-propenyl-1-trifluoroborate Usage And Synthesis

Uses

Potassium?trans-1-propenyltrifluoroborate can be used:

  • As a substrate in the cross-coupling reactions with 2-(chloromethyl)-2,1-borazaronaphthalenes to yield allyl borazaronaphthalenes using a palladium catalyst.
  • In the synthesis of anethole dithiolethione-NH2 (ADT-NH2), which in turn is used to prepare a drug-H2S delivery system.
  • To prepare methyl (E)-2,2-dimethyl-5-(propen-1-yl)-4H-benzo[d][1,3]dioxine-7-carboxylate, a key intermediate for the synthesis of the alkaloid ampullosine.

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