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1-PENTENYLBORONIC ACID

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1-PENTENYLBORONIC ACID Basic information

Product Name:
1-PENTENYLBORONIC ACID
Synonyms:
  • E-PENTEN-1-YLBORONIC ACID
  • (E)-1-PENTENYLBORONIC ACID
  • 1-PENTENYLBORONIC ACID
  • RARECHEM AH PB 0245
  • 1-penten-1-ylboronic acid
  • 1-Penthenylboronic Acid
  • 1-1-Pentenylboronic acid
  • 1-PENTENYLBORONIC ACID, 97+%
CAS:
104376-24-1
MF:
C5H11BO2
MW:
113.95
EINECS:
000-000-0
Product Categories:
  • blocks
  • BoronicAcids
  • Alkenyl
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Organoborons
  • Alkenyl Boronic Acids
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Organometallic Reagents
Mol File:
104376-24-1.mol
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1-PENTENYLBORONIC ACID Chemical Properties

Melting point:
100-105 °C (lit.)
Boiling point:
209.9±23.0 °C(Predicted)
Density 
0.936±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
pka
9.81±0.43(Predicted)
BRN 
2038297
CAS DataBase Reference
104376-24-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26-26 37/39
WGK Germany 
3
HS Code 
29310099

MSDS

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1-PENTENYLBORONIC ACID Usage And Synthesis

Chemical Properties

White shinying small flakes

Uses

Reactant for:• ;Synthesis of 8-alkenylborondipyrromethene dyes via Liebeskind-Srogl cross-coupling starting from 8-thiomethyl-substituted BODIPY1• ;Rhodium and palladium catalyzed substitution reactions with enyne acetates and carbonates2• ;Halogenation and protodeauration reactions of organogold phosphine complexes3• ;Lewis acid catalyzed Nazarov reaction4• ;Palladium-catalyzed tandem intramolecular C-N and intermolecular Suzuki coupling process5,6

Uses

Reactant for:

  • Synthesis of 8-alkenylborondipyrromethene dyes via Liebeskind-Srogl cross-coupling starting from 8-thiomethyl-substituted BODIPY
  • Rhodium and palladium catalyzed substitution reactions with enyne acetates and carbonates
  • Halogenation and protodeauration reactions of organogold phosphine complexes
  • Lewis acid catalyzed Nazarov reaction
  • Palladium-catalyzed tandem intramolecular C-N and intermolecular Suzuki coupling process

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