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Vinylboronic anhydride pyridine complex_Molecular_structure_CAS_442850-89-7)
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Vinylboronic anhydride pyridine complex

Catalog No. 637998 Name Sigma Aldrich
CAS Number 442850-89-7 Website http://www.sigmaaldrich.com
M. F. C11H14B3NO3 Telephone 1-800-521-8956
M. W. 240.66676 Fax
Purity 95% Email
Storage Chembase ID: 91517

SYNONYMS

Title
乙烯硼酐吡啶络合物
IUPAC name
pyridine; triethenyl-1,3,5,2,4,6-trioxatriborinane
IUPAC Traditional name
pyridine; triethenyl-1,3,5,2,4,6-trioxatriborinane
Synonyms
2,4,6-三乙烯基环硼氧烷吡啶络合物
Trivinylcyclotriboroxane pyridine complex
Trivinyl-boroxin pyridine complex
2,4,6-Trivinylcyclotriboroxane pyridine complex

DATABASE IDS

MDL Number MFCD03839940
PubChem SID 24882902
CAS Number 442850-89-7

PROPERTIES

Empirical Formula (Hill Notation) C6H9B3O3 · C5H5N
Purity 95%
Flash Point 80 °C
Flash Point 176 °F
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H319
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P305 + P351 + P338
Risk Statements 36
Safety Statements 26
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling1,2
• Stereoselective synthesis via Palladium-catalyzed carboamination3
• Alkyl-connected 2-amino-6-vinylpurine (AVP) crosslinking agent to cytosine base in RNA4
• Kaiser oxime resin-derived palladacycle as a recoverable polymeric precatalyst in Suzuki-Miyaura cross-coupling reactions in aqueous media5
• Kinetic resolution of phosphoryl and sulfonyl esters of binaphthol derivatives via Pd-catalyzed alcoholysis of their vinyl ethers6
• Stereoselective isomerization of N-allyl aziridines into Z-enamines by using rhodium hydride catalysis7
• Kinetic resolution of axially chiral biaryl derivatives via palladium/chiral diamine ligand-catalyzed alcoholysis8
• Transition metal-catalyzed alkenylation of aziridines, cycloaddition and thermal rearrangement reactions9
• Intramolecular Heck reaction strategy for synthesis of functionalized tetrahydroanthracenes10 Reagent used for Preparation of
• BACE-1 inhibitors and SAR of cyclic sulfone hydroxyethylamines11
• Distorted spiropentanes1
• Small molecule bradykinin B2 receptor antagonists in angioedema therapy12
• Enol Ethers13
• Styryl cyclobutanone
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura cross-coupling1,2
• Stereoselective synthesis via Palladium-catalyzed carboamination3
• Alkyl-connected 2-amino-6-vinylpurine (AVP) crosslinking agent to cytosine base in RNA4
• Kaiser oxime resin-derived palladacycle as a recoverable polymeric precatalyst in Suzuki-Miyaura cross-coupling reactions in aqueous media5
• Kinetic resolution of phosphoryl and sulfonyl esters of binaphthol derivatives via Pd-catalyzed alcoholysis of their vinyl ethers6
• Stereoselective isomerization of N-allyl aziridines into Z-enamines by using rhodium hydride catalysis7
• Kinetic resolution of axially chiral biaryl derivatives via palladium/chiral diamine ligand-catalyzed alcoholysis8
• Transition metal-catalyzed alkenylation of aziridines, cycloaddition and thermal rearrangement reactions9
• Intramolecular Heck reaction strategy for synthesis of functionalized tetrahydroanthracenes10 Reagent used for Preparation of
• BACE-1 inhibitors and SAR of cyclic sulfone hydroxyethylamines11
• Distorted spiropentanes1
• Small molecule bradykinin B2 receptor antagonists in angioedema therapy12
• Enol Ethers13
• Styryl cyclobutanone

REFERENCES