ChemicalBook--->CAS DataBase List--->1073354-41-2

1073354-41-2

1073354-41-2 Structure

1073354-41-2 Structure
IdentificationBack Directory
[Name]

2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE
[CAS]

1073354-41-2
[Synonyms]

2-Pyrrolidinopyridine-3-boronic acid, pinacol ester
2-(PYRROLIDIN-1-YL)PYRIDINE-3-BORONIC ACID PINACOL ESTER
2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, 95%
2-(1-Pyrrolidino)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE
2-(Pyrrolidin-l-y l)-3-(4,4,5,5-tetramethyl-l ,3.2-dioxaborolan-2-yl)pyridine
Pyridine, 2-(1-pyrrolidinyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C15H23BN2O2
[MDL Number]

MFCD06798280
[MOL File]

1073354-41-2.mol
[Molecular Weight]

274.17
Chemical PropertiesBack Directory
[Melting point ]

76-78°
[Boiling point ]

406.0±30.0 °C(Predicted)
[density ]

1.09±0.1 g/cm3(Predicted)
[form ]

solid
[pka]

7.05±0.31(Predicted)
[Water Solubility ]

Insoluble in water. Soluble in organic solvents.
[InChI]

1S/C15H23BN2O2/c1-14(2)15(3,4)20-16(19-14)12-8-7-9-17-13(12)18-10-5-6-11-18/h7-9H,5-6,10-11H2,1-4H3
[InChIKey]

RKTXCUGUPDEZHR-UHFFFAOYSA-N
[SMILES]

CC(O1)(C)C(C)(C)OB1C2=CC=CN=C2N3CCCC3
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Danger
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

WGK 3
[HS Code ]

2933998090
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Hazard InformationBack Directory
[Uses]

2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, is used as a main benefits of the use of boronic esters in Suzuki-Miyaura cross-couplings- Enabling the coupling of organoboronic acids that are sensitive to hydrolytic deboronation. It includes other additional application such as a number of chiral boronic esters, such as the ones illustrated hereafter, have been used as inducers in stereoselective reactions.
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