1269508-31-7 Usage
Description
2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine is a complex organic compound with a triazine core and phenyl and dioxaborolan-2-yl substituents. It is characterized by its unique molecular structure and properties, making it a valuable intermediate in various chemical reactions.
Uses
Used in Organic Synthesis:
2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows it to participate in a wide range of reactions, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Laboratory Research and Development:
In the laboratory setting, 2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine is used as a research tool to explore new chemical reactions and develop innovative synthetic methods. Its unique properties and reactivity make it an attractive candidate for studying reaction mechanisms and optimizing reaction conditions.
Used in Chemical Production Processes:
2,4-Diphenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine is also utilized in industrial chemical production processes. Its role as an intermediate allows for the efficient synthesis of target compounds on a larger scale, contributing to the manufacturing of various products across different industries.
Synthesis
15.0 g of 2-(3-Bromophenyl)-4,6-diphenyl-l,3,5-
triazine (32.4 mmol), 12.3 g of bis(pinacolato)diboron (48.6
mmol), 529 mg of Pd(dppf)Cl2.CH2Cl2 (0.647 mmol), 9.53
g of potassium acetate (97.1 mmol) and 323 ml of dioxane
were put into a 1-neck round flask and reacted under reflux
at 90° C. for 12 hours. After completion of the reaction, the solvent was removed under reduced pressure. The produced
solid was dissolved in dichloromethane and then filtered
through a Celite filter and washed with dichloromethane.
The solvent was removed under reduced pressure and the
resultant compound was crystallized with methanol to obtain
16.0 g of solid compound (intermediate 6) (yield: 96.8%).
Check Digit Verification of cas no
The CAS Registry Mumber 1269508-31-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,5,0 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1269508-31:
(9*1)+(8*2)+(7*6)+(6*9)+(5*5)+(4*0)+(3*8)+(2*3)+(1*1)=177
177 % 10 = 7
So 1269508-31-7 is a valid CAS Registry Number.
1269508-31-7Relevant articles and documents
Organic compound and organic electroluminescent device containing same
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, (2021/05/05)
The invention relates to an organic compound, which is characterized by having a structure as shown in (1), wherein L1 and L2 are respectively and independently selected from a single bond, a substituted or unsubstituted C6-C30 arylene group or a substituted or unsubstituted C3-C30 heteroarylene group; Arl and Ar2 are respectively and independently selected from a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; R is halogen, a cyano group, an alkyl group, a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; and n represents an integer of 0-3.
POLYCYCLIC COMPOUND, MATERIAL FOR AN ORGANIC ELECTROLUMINESCENCE DEVICE AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE POLYCYCLIC COMPOUND
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Paragraph 0113; 0264, (2021/07/02)
Specific polycyclic compounds represented by formula (la) or (lb), a material for an organic electroluminescence device comprising said specific polycyclic compound, an organic electroluminescence device comprising said specific polycyclic compound, an el
Nitrogen-containing compound, electronic element, and electronic device
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Paragraph 0161; 0166; 0167; 0169; 0170; 0171; 0172, (2020/12/30)
The invention belongs to the field of organic light-emitting materials, and provides a nitrogen-containing compound, an electronic element and an electronic device, the structure of the nitrogen-containing compound is shown as a chemical formula 1, X1, X2 and X3 are independently selected from CH or N respectively, and at least one of X1, X2 and X3 is N; Ar1 and Ar2 are each independently selectedfrom a substituted or unsubstituted aryl group having 6-40 carbon atoms or the like; and the nitrogen-containing compound can improve the performance of an electronic component.
