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1-Phenylvinylboronic acid, neopentyl glycol ester, is an organoboron compound that serves as a reagent in the Suzuki-Miyaura coupling reaction. It is characterized by its stability, being both air-stable and moisture-stable, and is extensively utilized in the pharmaceutical and agrochemical industries. This boronic acid reagent is highly valued for its capacity to form carbon-carbon bonds, which is instrumental in the synthesis of complex organic molecules. The neopentyl glycol ester derivative of 1-PHENYLVINYLBORONIC ACID, NEOPENTYL GLYCOL ESTER further improves its solubility and stability, making it a versatile reagent for a range of organic transformations.

938080-25-2

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938080-25-2 Usage

Uses

Used in Pharmaceutical Industry:
1-Phenylvinylboronic acid, neopentyl glycol ester, is used as a reagent for the Suzuki-Miyaura coupling reaction to facilitate the creation of biaryl compounds. This is crucial for the synthesis of complex organic molecules that are integral to the development of new pharmaceuticals.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Phenylvinylboronic acid, neopentyl glycol ester, is employed as a reagent for the same purpose, enabling the synthesis of complex organic molecules that are vital for the development of new agrochemicals.
Used in Organic Synthesis:
1-Phenylvinylboronic acid, neopentyl glycol ester, is used as a reagent for the construction of complex organic molecules through the formation of carbon-carbon bonds. Its use in conjunction with palladium catalysts allows for the coupling of aryl and vinyl halides or triflates, contributing to a broad spectrum of organic transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 938080-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,8,0,8 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 938080-25:
(8*9)+(7*3)+(6*8)+(5*0)+(4*8)+(3*0)+(2*2)+(1*5)=182
182 % 10 = 2
So 938080-25-2 is a valid CAS Registry Number.

938080-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-2-(1-phenylethenyl)-1,3,2-dioxaborinane

1.2 Other means of identification

Product number -
Other names 5,5-DIMETHYL-2-(1-PHENYLVINYL)-1,3,2-DIOXABORINANE

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:938080-25-2 SDS

938080-25-2Relevant academic research and scientific papers

Nickel-Catalyzed Regioselective Alkenylarylation of γ,δ-Alkenyl Ketones via Carbonyl Coordination

Aryal, Vivek,Dhungana, Roshan K.,Giri, Ramesh,Lakomy, Margaret G.,Niroula, Doleshwar,Sapkota, Rishi R.

supporting information, p. 19092 - 19096 (2021/08/09)

We disclose a nickel-catalyzed reaction, which enabled us to difunctionalize unactivated γ,δ-alkenes in ketones with alkenyl triflates and arylboronic esters. The reaction was made feasible by the use of 5-chloro-8-hydroxyquinoline as a ligand along with

Ruthenium-Catalyzed Monoalkenylation of Aromatic Ketones by Cleavage of Carbon-Heteroatom Bonds with Unconventional Chemoselectivity

Kondo, Hikaru,Akiba, Nana,Kochi, Takuya,Kakiuchi, Fumitoshi

supporting information, p. 9293 - 9297 (2015/08/06)

Ruthenium-catalyzed selective monoalkenylation of ortho C-O or C-N bonds of aromatic ketones was achieved. The reaction allowed the direct comparison of the relative reactivities of the cleavage of different carbon-heteroatom bonds, thus suggesting an unc

Nickel-catalysed carboxylation of organoboronates

Makida, Yusuke,Marelli, Enrico,Slawin, Alexandra M. Z.,Nolan, Steven P.

supporting information, p. 8010 - 8013 (2014/07/08)

A nickel/N-heterocyclic carbene (NHC) catalysed carboxylation of aryl-, heteroaryl- and alkenylboronates, affording the corresponding carboxylic acids, has been developed. This transformation proceeds under one atmosphere of CO 2 with a broad range of substrates and exhibits good functional group compatibility. the Partner Organisations 2014.

Copper(I)-catalyzed carboxylation of aryl- and alkenylboronic esters

Takaya, Jun,Tadami, Satoshi,Ukai, Kazutoshi,Iwasawa, Nobuharu

supporting information; experimental part, p. 2697 - 2700 (2009/05/26)

(Chemical Equation Presented) The copper(I)-catalyzed carboxylation reaction of aryl- and alkenylboronic esters proceeded smoothly under CO 2 to give the corresponding carboxylic acid in good yield. This reaction showed wide generality with higher functional group tolerance compared to the corresponding Rh(I)-catalyzed reaction.

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