267-94-7

Upstream product

• 77287-34-4 formamide 
• 24171-03-7 2,5-Diamino-1,4-benzenediol bis hydrochloride 
• 122-51-0 orthoformic acid triethyl ester 
• 10325-89-0 2,5-diamino-1,4-benzenediol 

Downstream Products

• 72129-95-4 3,3'-bis-(4-nitro-phenyl)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-propenone 
• 68579-07-7 2,2'-bis-(4-nitro-phenoxy)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68579-10-2 2,2'-bis-(2-chloro-phenoxy)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68579-09-9 2,2'-bis-(2-nitro-phenoxy)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 72129-96-5 3,3'-bis-(4-hydroxy-phenyl)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-propenone 
• 72129-92-1 3,3'-bis-(2-hydroxy-phenyl)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-propenone 
• 72129-94-3 3,3'-bis-(4-dimethylamino-phenyl)-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-propenone 
• 68578-93-8 2,2'-bis-benzylidenehydrazino-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-98-3 2,2'-bis-[(4-hydroxy-benzylidene)-hydrazino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-95-0 2,2'-bis-[(2-hydroxy-benzylidene)-hydrazino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-91-6 2,2'-bis-[((1S,2R)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-94-9 2,2'-bis-[(4-methoxy-benzylidene)-hydrazino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-96-1 2,2'-bis-[(4-dimethylamino-benzylidene)-hydrazino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 
• 68578-97-2 2,2'-bis-[(4-nitro-benzylidene)-hydrazino]-1,1'-benzo[1,2-d;4,5-d']bisoxazole-2,6-diyl-bis-ethanone 

Relevant academic research and scientific papers

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to: a compound which is represented by chemical formula I and can be applied to a hole injection layer, a hole transport layer, or a light efficiency improving layer of a device to implement an organic light emitting device h

An efficient synthesis of 2,6-disubstituted benzobisoxazoles: New building blocks for organic semiconductors

(Chemical Equation Presented) 2,6-Disubstituted benzobisoxazoles have been synthesized by a highly efficient reaction of diaminobenzene diols with various orthoesters. The scope of this new reaction for the synthesis of substituted benzobisoxazoles has been investigated using four different orthoesters. The utility of these compounds as building blocks for the synthesis of conjugated polymers is demonstrated.