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4-(4-Pyridinyl)phenylboronic acid pinacol ester is a chemical compound that belongs to the class of boronic acid esters. It is characterized by the presence of a boronic acid group, which makes it a valuable building block for various organic synthesis applications. 4-(4-Pyridinyl)phenylboronic acid pinacol ester is particularly useful in the preparation of pharmaceuticals, agrochemicals, and materials, playing a crucial role in the advancement of organic chemistry and drug discovery.

1009033-87-7

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1009033-87-7 Usage

Uses

Used in Organic Synthesis:
4-(4-Pyridinyl)phenylboronic acid pinacol ester is used as a reagent in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and materials. Its boronic acid group allows it to participate in Suzuki-Miyaura cross-coupling reactions, which are widely used in the construction of carbon-carbon bonds essential in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-(4-Pyridinyl)phenylboronic acid pinacol ester is used as a building block for the development of new drugs for various therapeutic areas. Its unique structure and reactivity make it a promising candidate for the design and synthesis of novel pharmaceutical agents with potential applications in treating various diseases and conditions.
Used in Pharmaceutical Industry:
4-(4-Pyridinyl)phenylboronic acid pinacol ester is used as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its involvement in Suzuki-Miyaura cross-coupling reactions enables the efficient construction of complex molecular frameworks, which are often found in potent and selective drug molecules.
Used in Agrochemical Industry:
4-(4-Pyridinyl)phenylboronic acid pinacol ester is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity in cross-coupling reactions allows for the creation of novel agrochemical agents with improved efficacy and selectivity, contributing to more effective and sustainable agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 1009033-87-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,0,3 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1009033-87:
(9*1)+(8*0)+(7*0)+(6*9)+(5*0)+(4*3)+(3*3)+(2*8)+(1*7)=107
107 % 10 = 7
So 1009033-87-7 is a valid CAS Registry Number.

1009033-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine

1.2 Other means of identification

Product number -
Other names 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine

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:1009033-87-7 SDS

1009033-87-7Relevant academic research and scientific papers

Evolution from Tunneling to Hopping Mediated Triplet Energy Transfer from Quantum Dots to Molecules

Huang, Zhiyuan,Xu, Zihao,Huang, Tingting,Gray, Victor,Moth-Poulsen, Kasper,Lian, Tianquan,Tang, Ming Lee

supporting information, p. 17581 - 17588 (2020/11/12)

Efficient energy transfer is particularly important for multiexcitonic processes like singlet fission and photon upconversion. Observation of the transition from short-range tunneling to long-range hopping during triplet exciton transfer from CdSe nanocrystals to anthracene is reported here. This is firmly supported by steady-state photon upconversion measurements, a direct proxy for the efficiency of triplet energy transfer (TET), as well as transient absorption measurements. When phenylene bridges are initially inserted between a CdSe nanocrystal donor and anthracene acceptor, the rate of TET decreases exponentially, commensurate with a decrease in the photon upconversion quantum efficiency from 11.6% to 4.51% to 0.284%, as expected from a tunneling mechanism. However, as the rigid bridge is increased in length to 4 and 5 phenylene units, photon upconversion quantum efficiencies increase again to 0.468% and 0.413%, 1.5-1.6 fold higher than that with 3 phenylene units (using the convention where the maximum upconversion quantum efficiency is 100%). This suggests a transition from exciton tunneling to hopping, resulting in relatively efficient and distance-independent TET beyond the traditional 1 nm Dexter distance. Transient absorption spectroscopy is used to confirm triplet energy transfer from CdSe to transmitter, and the formation of a bridge triplet state as an intermediate for the hopping mechanism. This first observation of the tunneling-to-hopping transition for long-range triplet energy transfer between nanocrystal light absorbers and molecular acceptors suggests that these hybrid materials should further be explored in the context of artificial photosynthesis.

Discovery of potent, orally bioavailable, small-molecule inhibitors of WNT signaling from a cell-based pathway screen

Adeniji-Popoola, Olajumoke,Aherne, Wynne,Blagg, Julian,Box, Gary,Clarke, Paul A.,Court, William,Crumpler, Simon,Dale, Trevor,De Haven Brandon, Alexis,Eccles, Suzanne A.,Esdar, Christina,Georgi, Katrin,Henley, Alan T.,Hobbs, Steve,Leuthner, Birgitta,Mallinger, Aurlie,Ortiz-Ruiz, Maria-Jesus,Pichowicz, Mark,Poeschke, Oliver,Raynaud, Florence,Rohdich, Felix,Schiemann, Kai,Smith, Elizabeth,Stieber, Frank,Stubbs, Mark,Tepoele, Robert,Thai, Ching,Valenti, Melanie,Waalboer, Dennis,Wienke, Dirk,Wood, Bozena,Workman, Paul

supporting information, p. 1717 - 1735 (2015/04/27)

WNT signaling is frequently deregulated in malignancy, particularly in colon cancer, and plays a key role in the generation and maintenance of cancer stem cells. We report the discovery and optimization of a 3,4,5-trisubstituted pyridine 9 using a high-throughput cell-based reporter assay of WNT pathway activity. We demonstrate a twisted conformation about the pyridine-piperidine bond of 9 by small-molecule X-ray crystallography. Medicinal chemistry optimization to maintain this twisted conformation, cognisant of physicochemical properties likely to maintain good cell permeability, led to 74 (CCT251545), a potent small-molecule inhibitor of WNT signaling with good oral pharmacokinetics. We demonstrate inhibition of WNT pathway activity in a solid human tumor xenograft model with evidence for tumor growth inhibition following oral dosing. This work provides a successful example of hypothesis-driven medicinal chemistry optimization from a singleton hit against a cell-based pathway assay without knowledge of the biochemical target.

OLEFIN SUBSTITUTED OXINDOLES HAVING AMPK ACTIVITY

-

Page/Page column 104, (2015/01/07)

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

3-(PYRAZOLYL)-1H-PYRROLO[2,3-b]PYRIDINE DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 42; 43; 25, (2014/01/18)

The present application relates to novel 3-(pyrazolyl)-lH-pyrrolo[2,3-b]pyridine derivatives of formula (I), as protein kinase inhibitors. The invention particularly relates to compounds of formula (I), preparation of compounds and pharmaceutical compositions thereof. The invention further relates to pharmaceutically acceptable salts and compositions comprising the said novel 3-(pyrazolyl)-lH-pyrrolo[2,3-b]pyridine derivatives and their use in the treatment of various disorders.

Novel four-pyridylbenzene-armed biphenyls as electron-transport materials for phosphorescent OLEDs

Su, Shi-Jian,Tanaka, Daisaku,Li, Yan-Jun,Sasabe, Hisahiro,Takeda, Takashi,Kido, Junji

supporting information; experimental part, p. 941 - 944 (2009/04/07)

A series of four-pyridylbenzene-armed biphenyl derivatives were designed and synthesized as an electron-transport and exciton- and hole-block layer for the fac-tris(2-phenylpyridine)iridium (lr(PPy)3)-based green phosphorescent organic light-em

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