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

  • CID 53357723
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  • 5-methoxy-7-(methoxymethoxy)-2H-chromene-3-carbaldehyde
  • N-(1-cyanobutyl)-5-(4-fluorophenyl)-5-oxopentanamide
  • N-(1-cyanopropyl)-3-(1,1-dioxo-1lambda6,2-thiazolidin-2-yl)benzamide
  • (E)-N-(1-methyl-5-oxopyrrolidin-3-yl)-2-(p-tolyl)ethenesulfonamide
  • tert-Butyl 4-[(5-bromo-2-fluorobenzene)sulfonyl]piperazine-1-carboxylate
  • 3-chloro-N-(1-methyl-5-oxopyrrolidin-3-yl)benzene-1-sulfonamide
  • N-(1-cyano-1,2-dimethylpropyl)-2-[(1-ethyl-4-oxo-1,4-dihydropyrimidin-2-yl)sulfanyl]acetamide
  • (4-Benzyloxy-3-trifluoromethyl-pyridin-2-yl)-hydrazine
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