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TRANS-1-PROPEN-1-YLBORONIC ACID

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TRANS-1-PROPEN-1-YLBORONIC ACID Basic information

Product Name:
TRANS-1-PROPEN-1-YLBORONIC ACID
Synonyms:
  • TRANS-1-PROPEN-1-YLBORONIC ACID
  • [(1E)-prop-1-en-1-yl]boronic acid
  • Prop-1-en-1-ylboronic acid
  • (E)-prop-1-en-1-ylboronic acid
  • trans-1-Propen-1-ylboronic acid >=95.0%
  • (E)-1-propen-1-yl-boronicacid
  • (E)-Prop-1-enylboronic acid
  • trans-1-Propeneboronic acid
CAS:
7547-97-9
MF:
C3H7BO2
MW:
85.9
EINECS:
200-258-5
Product Categories:
  • BoronicAcids
  • Boric Acid| Boric Acid Ester| Potassium Trifluoroborate
  • blocks
  • Alkenyl
  • Boronic Acids
  • Boronic Acids and Derivatives
Mol File:
7547-97-9.mol
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TRANS-1-PROPEN-1-YLBORONIC ACID Chemical Properties

Melting point:
123-127 °C(lit.)
Boiling point:
175.6±23.0 °C(Predicted)
Density 
0.972 g/cm3(Temp: 19 °C)
storage temp. 
2-8°C
solubility 
Chloroform (Very Slightly, Heated), Methanol (Very Slightly)
form 
Solid
pka
9.80±0.43(Predicted)
color 
Pale Beige
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Safety Information

WGK Germany 
3
HS Code 
2931900090
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TRANS-1-PROPEN-1-YLBORONIC ACID Usage And Synthesis

Uses

Reactant for:

  • Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions
  • Cu(II)-mediated Ullmann-type coupling

Reactant for preparation of:
  • Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases
  • Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling
  • Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
  • Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones

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