663954-31-2 Usage
Uses
Used in Organic Synthesis:
2-P-TERPHENYLBORONIC ACID is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Catalysis:
In the field of catalysis, 2-P-TERPHENYLBORONIC ACID is utilized as a catalyst to accelerate chemical reactions, enhancing the efficiency and selectivity of processes in the synthesis of pharmaceuticals and other organic compounds.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
2-P-TERPHENYLBORONIC ACID is used as a key component in the Suzuki-Miyaura cross-coupling reaction, a method widely employed for the formation of carbon-carbon bonds, which is crucial for constructing molecular frameworks in organic chemistry.
Used in Material Development:
2-P-TERPHENYLBORONIC ACID is also used as a precursor in the development of new materials, leveraging its chemical properties to create innovative substances with potential applications in various industries.
Used in Pharmaceutical Development:
2-P-TERPHENYLBORONIC ACID is utilized in the pharmaceutical industry for the synthesis of new drugs, taking advantage of its reactivity and structural features to design and produce novel medicinal compounds.
Used in Fluorescence-Based Detection Methods:
Capitalizing on its fluorescent properties, 2-P-TERPHENYLBORONIC ACID is employed in fluorescence-based detection methods, serving as a marker or indicator in analytical chemistry for the identification and quantification of substances.
Check Digit Verification of cas no
The CAS Registry Mumber 663954-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,3,9,5 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 663954-31:
(8*6)+(7*6)+(6*3)+(5*9)+(4*5)+(3*4)+(2*3)+(1*1)=192
192 % 10 = 2
So 663954-31-2 is a valid CAS Registry Number.
663954-31-2Relevant academic research and scientific papers
Rh(III)-Catalyzed C-H Activation of Boronic Acid with Aryl Azide
Xu, Shiyang,Huang, Baoliang,Qiao, Guanyu,Huang, Ziyue,Zhang, Zhen,Li, Zongyang,Wang, Peng,Zhang, Zhenhua
supporting information, p. 5578 - 5582 (2018/09/25)
A Rh(III)-catalyzed C-H activation of boronic acid with aryl azide to obtain unsymmetric carbazoles, 1H-indoles, or indolines has been developed. The reaction constructs dual distinct C-N bonds via sp2/sp3 C-H activation and rhodium nitrene insertion. Synthetically, this approach represents an access to widely used carbazole derivatives. The practical application to CBP and unsymmetric TCTA derivatives has also been performed. Mechanistic experiments and DFT calculations demonstrate that a five-membered rhodacycle species is the key intermediate.
Rhodium-Catalyzed Oxidative Annulation of (2-Arylphenyl)boronic Acids with Alkynes: Selective Synthesis of Phenanthrene Derivatives
Nagata, Tomoya,Satoh, Tetsuya,Nishii, Yuji,Miura, Masahiro
supporting information, p. 1707 - 1710 (2016/07/06)
A rhodium-catalyzed annulative coupling of (2-arylphenyl)boronic acids with alkynes has been developed for the facile construction of phenanthrene frameworks. The reaction proceeded without external bases, and dioxygen worked as a terminal oxidant. Deuter
