219834-96-5 Usage
Description
(2-(Benzyloxy)naphthalen-1-yl)boronic acid, also known as 2-benzyloxy-1-naphthylboronic acid, is a boronic acid derivative with the molecular formula C18H15BO3. It is a naphthalene analog with a benzyloxy group attached to the 2-position, making it a versatile reagent in organic chemistry.
Used in Pharmaceutical Industry:
(2-(Benzyloxy)naphthalen-1-yl)boronic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction, enabling the creation of complex molecular structures with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (2-(Benzyloxy)naphthalen-1-yl)boronic acid serves as a building block for the development of new agrochemicals. Its ability to form carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction aids in the synthesis of novel compounds with potential applications in crop protection and pest control.
Used in Materials Science:
(2-(Benzyloxy)naphthalen-1-yl)boronic acid is utilized in materials science for the synthesis of advanced materials with unique properties. Its involvement in the Suzuki-Miyaura cross-coupling reaction allows for the creation of new materials with potential applications in various fields, such as electronics, energy storage, and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 219834-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,3 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 219834-96:
(8*2)+(7*1)+(6*9)+(5*8)+(4*3)+(3*4)+(2*9)+(1*6)=165
165 % 10 = 5
So 219834-96-5 is a valid CAS Registry Number.
219834-96-5Relevant articles and documents
Catalytic Enantioselective Synthesis of Axially Chiral Diarylmethylidene Indanones
Kumar, Prashant,Shirke, Rajendra P.,Yadav, Sonu,Ramasastry
, p. 4909 - 4914 (2021/06/30)
We describe the first atropselective Suzuki-Miyaura cross-coupling of β-keto enol triflates to access axially chiral (Z)-diarylmethylidene indanones (DAIs). The chemical, physical, and biological properties of DAIs are unknown, despite their being structurally similar to arylidene indanones, primarily due to the lack of racemic or chiral methods. Through this work, we demonstrate a general and efficient protocol for the racemic as well as the atropselective synthesis of (Z)-DAIs. An unusual intramolecular Morita-Baylis-Hillman reaction is utilized for the Z-selective synthesis of β-keto enol triflates.
Efficient synthesis of chiral 1,1′-binaphthalenes by the asymmetric suzuki-miyaura reaction: Dramatic synthetic improvement by simple purification of naphthylboronic acids
Genov, Miroslav,Almorin, Antonio,Espinet, Pablo
, p. 9346 - 9352 (2007/10/03)
Naphthylboronic acids prepared as reported in the literature are contaminated with HCl. A very simple purification prior to their use in Suzuki-Miyaura couplings has been found to be crucial, rendering efficient some reactions that had been reported in th
