(1E)-1-Propen-1-ylboronic acid

Modify Date: 2024-01-08 18:43:25

(1E)-1-Propen-1-ylboronic acid Structure
(1E)-1-Propen-1-ylboronic acid structure
Common Name (1E)-1-Propen-1-ylboronic acid
CAS Number 7547-97-9 Molecular Weight 85.897
Density 1.0±0.1 g/cm3 Boiling Point 175.6±23.0 °C at 760 mmHg
Molecular Formula C3H7BO2 Melting Point 123-127ºC(lit.)
MSDS Chinese USA Flash Point 60.0±22.6 °C

 Names

Name (E)-Prop-1-en-1-ylboronic acid
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 175.6±23.0 °C at 760 mmHg
Melting Point 123-127ºC(lit.)
Molecular Formula C3H7BO2
Molecular Weight 85.897
Flash Point 60.0±22.6 °C
Exact Mass 86.053909
PSA 40.46000
LogP 0.96
Vapour Pressure 0.4±0.7 mmHg at 25°C
Index of Refraction 1.422
Storage condition -20 °C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles9

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J. Med. Chem. 20th ed., 54 , 7299-7317, (2011)

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Selective palladium-catalyzed C-F activation/carbon-carbon bond formation of polyfluoroaryl oxazolines.

J. Org. Chem. 4th ed., 77 , 1798-1804, (2012)

A selective palladium-catalyzed Suzuki-Miyaura coupling reaction of polyfluorophenyl oxazolines through ortho C-F activation is described. It was found that reactions with DPPF as the ligand occurred ...

Highly selective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids: a novel route to substituted 1,3-dienes.

Org. Lett. 12 , 3610-3613, (2010)

A highly regio- and stereoselective nickel-catalyzed three-component coupling of alkynes with enones and alkenyl boronic acids to afford highly substituted 1,3-dienes is described. The reaction can al...

 Synonyms

(1E)-1-Propen-1-ylboronic acid
[(E)-prop-1-enyl]boronic acid
Boronic acid, B-[(1E)-1-propen-1-yl]-