330793-45-8 Usage
Description
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID, with the chemical formula C18H16BNO3, is an organoboronic acid compound. It is widely used in organic synthesis and serves as a building block for the preparation of pharmaceuticals, agrochemicals, and organic materials. The presence of its boronic acid functional group allows it to act as a reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This versatile compound has potential applications in the development of new drugs and materials, as well as in the synthesis of complex organic molecules for various industrial purposes.
Uses
Used in Organic Synthesis:
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID is used as a building block for the synthesis of various organic compounds due to its reactivity and ability to form carbon-carbon bonds.
Used in Pharmaceutical Industry:
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID is used as a key intermediate in the development of new drugs, contributing to the creation of innovative pharmaceuticals with improved therapeutic properties.
Used in Agrochemical Industry:
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Material Science:
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID is used as a component in the development of advanced materials with specific properties, such as conductivity, stability, or optical characteristics.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
(4-PHENYLAMINOCARBONYLPHENYL)BORONIC ACID is used as a reagent in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds, enabling the synthesis of complex organic molecules for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 330793-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,7,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 330793-45:
(8*3)+(7*3)+(6*0)+(5*7)+(4*9)+(3*3)+(2*4)+(1*5)=138
138 % 10 = 8
So 330793-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H12BNO3/c16-13(15-12-4-2-1-3-5-12)10-6-8-11(9-7-10)14(17)18/h1-9,17-18H,(H,15,16)
330793-45-8Relevant articles and documents
Discovery of thieno[3,2-c]pyridin-4-amines as novel Bruton's tyrosine kinase (BTK) inhibitors
Zhao, Xinge,Xin, Minhang,Wang, Yazhou,Huang, Wei,Jin, Qiu,Tang, Feng,Wu, Gang,Zhao, Yong,Xiang, Hua
, p. 6059 - 6068 (2015)
A novel series of BTK inhibitors bearing thieno[3,2-c]pyridin-4-amine framework as the core scaffold were designed, synthesized and well characterized. In this paper, twenty one compounds displayed variant inhibitory activities against BTK in vitro, and c
Thieno [3, 2 - c] pyridine compound, its preparation method and application
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Paragraph 0237; 0238; 0239; 0250, (2018/09/02)
The invention relates to a thieno-[3,2-c] pyridine type compound and an application thereof. The compound has a structure shown by a formula (I) in the specification. The compound of which the structure is shown by the formula (I), provided by the invention has a very good effect of inhibiting the activity of Bruton kinase. The invention also relates to the application of the compound in preventing and/or treating diseases which are improved by virtue of BTK (Bruton tyrosine kinase) activity inhibition.
Pyrazolopyrimidines as therapeutic agents
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, (2008/06/13)
The present invention is directed to pyrazolopyrimidine derivatives of formula (I) wherein the substituents are defined herein, which are useful as kinase inhibitors and as such are useful for affecting angiogenesis and diseases and conditions associated with angiogenesis.