938080-25-2 Usage
General Description
1-Phenylvinylboronic acid, neopentyl glycol ester, is an organoboron compound used in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction. It is a stable, air-stable, and moisture-stable boronic acid reagent that is widely used in the pharmaceutical and agrochemical industries. 1-PHENYLVINYLBORONIC ACID, NEOPENTYL GLYCOL ESTER is known for its ability to form carbon-carbon bonds, making it a valuable tool for the construction of complex organic molecules. It is typically used in conjunction with palladium catalysts to facilitate the coupling of aryl and vinyl halides or triflates, enabling the creation of a wide range of biaryl compounds. Its neopentyl glycol ester derivative enhances its solubility and stability, making it a useful reagent for a variety 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.
938080-25-2Relevant articles and documents
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
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.
