320381-26-8 Usage
Description
(2-phenylnaphthalen-1-yl)boronic acid is a boronic acid derivative with the molecular formula C16H13BO2. It features a naphthalene ring and a phenyl group attached to the boron atom, making it a versatile compound in various chemical applications.
Uses
Used in Organic Synthesis:
(2-phenylnaphthalen-1-yl)boronic acid is used as a building block for the construction of various biaryl and heteroaryl compounds, which are important in the synthesis of pharmaceuticals, agrochemicals, and functional materials.
Used in Cross-Coupling Reactions:
(2-phenylnaphthalen-1-yl)boronic acid is used as a reagent in cross-coupling reactions to form carbon-carbon bonds, which are crucial for the synthesis of complex organic molecules and the development of new chemical entities.
Used in Suzuki-Miyaura Coupling Reactions:
(2-phenylnaphthalen-1-yl)boronic acid is used as a coupling partner in Suzuki-Miyaura coupling reactions, a widely used method for the formation of carbon-carbon bonds, particularly in the synthesis of biaryl compounds.
Used in Medicinal Chemistry:
(2-phenylnaphthalen-1-yl)boronic acid is used as a structural component in the design and synthesis of new pharmaceutical agents, taking advantage of its unique reactivity and structural properties.
Used in Material Science:
(2-phenylnaphthalen-1-yl)boronic acid is used in the development of new materials with specific properties, such as optoelectronic materials, sensors, and catalysts, due to its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 320381-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,3,8 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 320381-26:
(8*3)+(7*2)+(6*0)+(5*3)+(4*8)+(3*1)+(2*2)+(1*6)=98
98 % 10 = 8
So 320381-26-8 is a valid CAS Registry Number.
320381-26-8Relevant articles and documents
Stereochemical stability differences between axially chiral 6-Aryl-substituted picolinic esters and their benzoic ester derivatives: Sp2 N: Vs. sp2 CH in CH3, C6 H5, and CH3 O ortho-substitution effect
Tanaka, Shinji,Suzuki, Yusuke,Matsushita, Masaharu,Kitamura, Masato
, p. 1726 - 1734 (2016/01/26)
An axially chiral naphthyl-substituted picolinic acid (R-Naph-PyCOOH) or its allyl ester (R-Naph-PyCOOAll) acts as an excellent ligand for catalytic asymmetric dehydrative intramolecular allylation. Towards the future development of a high performance cat
