929203-04-3

Basic information

• Product Name: 4-(3-Pyridinyl)phenylboronic acid pinacol ester
• Synonyms: 4-(3-PYRIDINYL)PHENYLBORONIC ACID PINACOL ESTER;1-(3-Pyridyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene;3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine;3-(4-Phenylboronic acid pinacol ester)pyridine;Pinacol 4-(pyridin-3-yl)phenylboronate
• CAS NO: 929203-04-3
• Molecular Formula: C₁₇H₂₀BNO₂
• Molecular Weight: 281.16
• Mol File: 929203-04-3.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 410.7±28.0 °C(Predicted)
• Appearance: /
• Density: 1.09
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 4.76±0.10(Predicted)
• CAS DataBase Reference: 4-(3-Pyridinyl)phenylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-Pyridinyl)phenylboronic acid pinacol ester(929203-04-3)
• EPA Substance Registry System: 4-(3-Pyridinyl)phenylboronic acid pinacol ester(929203-04-3)

Safety Data

• Hazardous Substances Data: 929203-04-3(Hazardous Substances Data)

Usage

General Description

4-(3-Pyridinyl)phenylboronic acid pinacol ester is a chemical compound that is commonly used as a reagent in organic synthesis. It is a boronic acid derivative with a pyridinyl group attached to a phenyl ring and a pinacol ester functional group. 4-(3-Pyridinyl)phenylboronic acid pinacol ester has been shown to be useful in Suzuki-Miyaura coupling reactions, which is a widely used method for forming carbon-carbon bonds in organic chemistry. The pinacol ester moiety provides increased stability and solubility, making it a valuable tool for the construction of complex organic molecules. Additionally, 4-(3-Pyridinyl)phenylboronic acid pinacol ester has been used in the development of pharmaceuticals, agrochemicals, and materials science research.

Upstream product

• 5957-97-1 4-(3'-pyridinyl)-1-chlorobenzene 
• 73183-34-3 bis(pinacol)diborane 
• 214360-73-3 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)aniline 
• 626-55-1 3-Bromopyridine 
• 106-50-3 1,4-phenylenediamine 
• 171364-83-3 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nitrobenzene 
• 100-01-6 4-nitro-aniline 
• 129013-83-8 3-(4-bromophenyl)pyridine 
• 589-87-7 1,4-bromoiodobenzene 
• 1692-25-7 3-pyridylboronic acid 
• 4385-75-5 4-(pyridine-3-yl)benzoic acid 

Downstream Products

• 1009033-95-7 3,5,3',5'-tetra(p-pyridin-3-yl)phenyl-[1,1']biphenyl 
• 1335471-11-8 tris(2,3,5,6-tetramethyl-4-(pyridin-3-yl)phenyl)borane 
• 921205-02-9 1,3,5-tris[4-(pyridin-3-yl)phenyl]benzene 
• 1383795-49-0 C₄₄H₂₈N₂ 

Relevant articles and documents

Compound with AMPK agonistic activity and preparation and application of prodrug thereof

The invention relates to a compound with AMPK agonistic activity and a prodrug thereof, and as well as a preparation method and medical application of a prodrug thereof. The compound has the structure shown in the formula (I), and the prodrug of the compound has the structure shown in the formula (II), wherein each group and the substituent are as defined in the specification. The invention discloses a preparation method of the compound and application of the compound in prevention and treatment AMPK related diseases, and the AMPK related diseases include, but are not limited to, energy metabolism abnormality related diseases. Neurodegenerative diseases and inflammation-related diseases and the like.

Phenylpyridine derivative (by machine translation)

[Problem] in a photoelectric conversion element, the heat resistance can be improved phenylpyridine derivative. (1) Represented by the formula [a] phenylpyridine derivative (A ring, B, C D and is, a pyridine ring, each of the carbon atoms contained in R1 - R11, hydrogen, straight-chain alkyl group, a branched alkyl group, an aryl group, such as one selected from binding. ). Figure 1 [drawing] (by machine translation)

Triaryl boron derivatives of pyridine as electron transporting materials for blue phosphorescent organic light-emitting diodes

Two duryl borane derivatives, tris(2,3,5,6-tetramethyl-4-(pyridin-3-yl)phenyl)borane (TDPB) and tris(2,3,5,6-tetramethyl-4'-(pyridin-3-yl)biphenyl-4-yl)borane (TDPPB), which contain heteroaromatic pyridine rings at peripheral positions were synthesized to