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2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE, also known as 2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, is a complex organic compound with a unique structure that features a pyrrolidine and a boron-containing dioxaborolane group. 2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE is particularly useful in chemical synthesis and has been found to have potential applications in various fields due to its unique reactivity and properties.

1073354-41-2

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1073354-41-2 Usage

Uses

Used in Chemical Synthesis:
2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE is used as a key intermediate in the synthesis of various organic compounds, particularly in the field of pharmaceuticals and materials science. Its unique structure allows for the formation of new bonds and the creation of complex molecular architectures.
Used in Suzuki-Miyaura Cross-Couplings:
One of the main benefits of using 2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester is its application in Suzuki-Miyaura cross-couplings. This is a widely used method in organic chemistry for the formation of carbon-carbon bonds, enabling the coupling of organoboronic acids that are sensitive to hydrolytic deboronation. The use of 2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE in such reactions leads to the formation of stable and functionalized products, which are valuable in the synthesis of various target molecules.
Used in Stereoselective Reactions:
2-(PYRROLIDIN-1-YL)-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE is also used as a chiral inducer in stereoselective reactions. Chiral boronic esters, such as the one described, have been employed to control the stereochemistry of the products formed in these reactions. This is particularly important in the synthesis of enantiomerically pure compounds, which are often required for biological activity and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1073354-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1073354-41:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*5)+(3*4)+(2*4)+(1*1)=132
132 % 10 = 2
So 1073354-41-2 is a valid CAS Registry Number.
InChI:InChI=1/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

1073354-41-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H27190)  2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, 95%   

  • 1073354-41-2

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H27190)  2-(1-Pyrrolidinyl)pyridine-3-boronic acid pinacol ester, 95%   

  • 1073354-41-2

  • 1g

  • 3391.0CNY

  • Detail

1073354-41-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrrolidin-1-yl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2-Pyrrolidin-1-ylpyridine-3-boronic acid pinacol ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1073354-41-2 SDS

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