Vinylboronic anhydride pyridine complex

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Names

[ CAS No. ]:
442850-89-7

[ Name ]:
Vinylboronic anhydride pyridine complex

[Synonym ]:
MFCD03839940

Chemical & Physical Properties

[ Boiling Point ]:
78-80 ℃

[ Melting Point ]:
49 - 53 ℃

[ Molecular Formula ]:
C11H14B3NO3

[ Molecular Weight ]:
240.66700

[ Flash Point ]:
80 ℃ - 闭杯

[ Exact Mass ]:
241.12500

[ PSA ]:
40.58000

[ LogP ]:
1.77160

[ Storage condition ]:
-20 °C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

Articles

Transition metal-catalyzed synthesis and reactivity of N-alkenyl aziridines.

Org. Lett. 6th ed., 7 , 1161-1164, (2005)

[reaction: see text] Straightforward methods for palladium-catalyzed alkenylation of aziridines with alkenyl halides and copper-catalyzed alkenylation of aziridines with alkenyl boronic acids have bee...

Stereoselective isomerisation of N-allyl aziridines into geometrically stable Z enamines by using rhodium hydride catalysis.

Chemistry 3rd ed., 14 , 886-894, (2008)

In the presence of rhodium(I) hydride catalysts, tertiary N-allylamines are known to isomerise into E enamines. In contrast, we have recently found that N-allylaziridines isomerise to form Z enamines....

The alkyl-connected 2-amino-6-vinylpurine (AVP) crosslinking agent for improved selectivity to the cytosine base in RNA

Bioorg. Med. Chem. 8th ed., 18 , 2894-2901, (2010)

The ethylene-connected 2-amino-6-vinylpurine (AVP) crosslinking agent exhibited improved reactivity and selectivity to the cytosine base in RNA.


More Articles

Related Compounds

  • Methyl 7-bromo-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate
  • (2,2-Difluoroethyl)(propyl)amine
  • 2-butyl-2,3-dihydro-1H-isoindol-5-amine
  • 2-(3,5-Dichlorophenyl)-2,3-dihydro-1H-isoindol-4-amine
  • Tetrahydro-4-(methylamino)-2H-pyran-4-carbonitrile
  • 3-amino-1-[3-(1H-imidazol-1-yl)propyl]urea
  • Benzamide, 4-fluoro-N-[4-(methylamino)cyclohexyl]-
  • N-[(4-ethoxyphenyl)methyl]tetrahydropyran-4-amine
  • 2-[5-(Azetidin-3-yl)-1,2,4-oxadiazol-3-yl]pyrazine
  • 5-Bromo-2-iodo-N-ethyl benzamide
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