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

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

  • 3-Methyl-4-(piperidin-4-ylmethyl)aniline
  • (Z)-Ethyl 2-(2-fluoro-3-methoxyphenyl)-3-((phenoxycarbonyl)amino)but-2-enoate
  • N-[4-(2-aminopropan-2-yl)phenyl]methanesulfonamide
  • 1-(4-chloro-2-methoxyphenyl)-1H-imidazole
  • 3-(2,4-Difluorobenzyl)pyrrolidine
  • N-cyclopropyl-2-[[2-(dimethylamino)-2-methylpropyl]amino]acetamide
  • tert-butyl N-[2-amino-1-(1-ethyl-1H-imidazol-5-yl)ethyl]carbamate
  • 2-amino-1-(1-ethyl-1H-imidazol-5-yl)ethan-1-ol
  • 5-(Methanesulfinylmethyl)furan-2-carboxylic acid
  • 4-[(Phenylsulfinyl)methyl]benzenamine
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