943899-12-5 Usage
Uses
Used in Organic Synthesis:
(3-(diphenylamino)phenyl)boronic acid is used as a versatile building block for the development of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity contribute to the synthesis of complex organic molecules and materials.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
In the field of organic chemistry, (3-(diphenylamino)phenyl)boronic acid is used as a valuable reagent in the Suzuki-Miyaura cross-coupling reaction. This reaction is a widely used method for the formation of carbon-carbon bonds, facilitating the creation of new compounds and structures in organic synthesis.
Used in Pharmaceutical Development:
(3-(diphenylamino)phenyl)boronic acid is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its unique properties allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, (3-(diphenylamino)phenyl)boronic acid is employed as a building block for the synthesis of various agrochemicals, including pesticides and herbicides, contributing to the development of effective crop protection solutions.
Used in Material Science:
(3-(diphenylamino)phenyl)boronic acid is also used in material science for the synthesis of new materials with specific properties, such as conductivity, stability, or optical characteristics, which can be applied in various technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 943899-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,8,9 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 943899-12:
(8*9)+(7*4)+(6*3)+(5*8)+(4*9)+(3*9)+(2*1)+(1*2)=225
225 % 10 = 5
So 943899-12-5 is a valid CAS Registry Number.
943899-12-5Relevant articles and documents
Organic light-emitting diode materials
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Paragraph 0362; 0363, (2017/07/26)
Described herein are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moiety D, each moiety D is covalently attached to either the moiety B or the moiety A, and each moiety B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D, and B are defined herein.
Organic Compound and Organic Light Emitting Diode Devices using the same
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Paragraph 0086-0088, (2016/11/17)
The present invention relates to an organic compound and an organic light emitting diode device using same. The organic compound is selected from an aromatic ring compound, which is represented by Chemical formula wherein R is a substituted or unsubsituted alkyl group having C_1 to C_12; and A and B are symmetrically or asymmetrically bound to a 2-position and a 7-position of a fullerene core and are independently substituted or unsubstituted, and a heterogeneous ring compound. According to the present invention, efficiency of the organic light diode device can be increased; and driving voltages for the organic light diode device can be reduced.COPYRIGHT KIPO 2015
NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME
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Page/Page column 14, (2011/06/11)
Provided are organic electroluminescent compounds and organic electroluminescent device using the same of Chemical Formula I. The organic electroluminescent compounds according to the present invention exhibit high luminous efficiency and excellent life p
