1197989-80-2

Upstream product

• 1197993-09-1 3,3'-(5'-chloro-[1,1':3',1''-terphenyl]-3,3''-diyl)dipyridine 
• 1197993-07-9 C₃₄H₃₁BN₂O₂ 
• 939430-30-5 3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine 
• 591-18-4 1-Bromo-3-iodobenzene 
• 4422-32-6 3-(3'-bromophenyl)pyridine 
• 1692-25-7 3-pyridylboronic acid 
• 1233923-10-8 1,3-bis(3-pyridinephenyl)-5-(3-chlorophenyl)benzene 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 1197989-81-3 C₇₃H₄₉N₅ 
• 1197989-87-9 C₃₉H₂₆BrN₃ 
• 1197989-82-4 C₃₄H₂₅BN₂O₂ 

Relevant academic research and scientific papers

PROCESS FOR MAKING ORGANIC COMPOUNDS AND THE ORGANIC COMPOUNDS MADE THEREFROM

An organic compound of formula E is made from a process comprising: reacting a compound of formula A and a compound of formula B to form a compound of formula C; and reacting one of the compound of formula C and the compound of formula D with a first boro

ELECTRON-TRANSPORTING MATERIALS AND PROCESSES FOR MAKING THE SAME

Compound of formula C is made by reacting a compound of formula A with an pyridyl boronic acid or pyridyl borate ester to form a compound of formula B; and combining the compound of formula B with a pyridyl dihalide to form the compound of C; wherein Rsu

2,4,6-TRI-(HETEROARYLPHENYL)-PYRIDINES AND ELECTRON-TRANSPORTING MATERIALS COMPRISING THEM

Compounds of formula 1 may be used in optoelectronic devices wherein R1 and R2 are, independently at each occurrence, H, a C1-C20 aliphatic radical, a C3-C20 aromatic radical, or a C3-C20 cyeioaiiphatic radical; a is an integer ranging from 0-2; b is 1 or 2; c is an integer ranging from 0-4; and Ar1 and Ar2; are independently heteroaryl.