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Diethyl(3-pyridyl)borane

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Diethyl(3-pyridyl)borane Basic information
Product Name:Diethyl(3-pyridyl)borane
Synonyms:3-Diethylboranyl Pyridine;3-(DIETHYLBORYL)PYRIDINE;Diethyl(3-pyridyl)borane,95%;3-(diethylboryl)pyridine, Abiraterone intermediate;3-(diethyboryl)pyridine;Dithyl (3-Pyridyl)borane;Diethyl(3-pyridyl)borane,3-(Diethylboryl)pyridine;Diethyl(3-pyridyl)bo
CAS:89878-14-8
MF:C9H14BN
MW:147.03
EINECS:627-082-6
Product Categories:Organic boronic acid;Boranes;Nitrogen cyclic compounds;B (Classes of Boron Compounds);89878-14-8
Mol File:89878-14-8.mol
Diethyl(3-pyridyl)borane Structure
Diethyl(3-pyridyl)borane Chemical Properties
Melting point 172-175 °C(lit.)
Boiling point 205.9±22.0 °C(Predicted)
density 0.86±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka4.40±0.12(Predicted)
form Solid
color White to Almost white
Water Solubility Slightly soluble in water.
InChIInChI=1S/C9H14BN/c1-3-10(4-2)9-6-5-7-11-8-9/h5-8H,3-4H2,1-2H3
InChIKeyOJKBCQOJVMAHDX-UHFFFAOYSA-N
SMILESC1=NC=CC=C1B(CC)CC
CAS DataBase Reference89878-14-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Diethyl(3-pyridyl)borane Usage And Synthesis
Chemical PropertiesWhite to yellow solid
UsesReactant for: preparation of inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents, N-Methylation reactions of the pyridyl group, Palladium catalyzed amination reactions, intramolecular Heck reactions, Coupling reactions and Synthesis of trisubstituted pyrimidines from polyhalopyrimidines via Suzuki coupling.
UsesReactant for:
  • Preparation of inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents
  • N-Methylation reactions of the pyridyl group
  • Palladium catalyzed amination reactions
  • Intramolecular Heck reactions
  • Coupling reactions
  • Synthesis of trisubstituted pyrimidines from polyhalopyrimidines via Suzuki coupling
Usessuzuki reaction
reaction suitabilityreagent type: reductant
Synthesis

Reaction temperature 0 ~ 5 , reaction time 6h, diethylmethoxyborane drop time 30 min, material ratio n (3-bromopyridine): n (diethylmethoxyborane) for 0.9:1.0, material ratio n (isopropylmagnesium chloride): n (diethylmethoxyborane) for 1.0:1.0. In the optimal conditions of the process to produce the product is a white solid, melting point of 172 ~ 175 , yield of more than 81%. Under the optimal process conditions, the product is white solid with a melting point of 172175 and a yield of more than 81%.

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