861905-18-2

Upstream product

• 93777-26-5 5-bromo-2-fluorobenzaldehyde 
• 53857-57-1 5-bromo-1H-indazole 
• 98-80-6 phenylboronic acid 
• 591-50-4 iodobenzene 
• 710292-24-3 C₁₃H₁₀BrFN₂ 

Downstream Products

• 861905-23-9 3-fluoro-4-methyl-5-(1-phenyl-1H-indazol-5-yl)benzoic acid 
• 1134916-62-3 2-(2,4-dichloro-phenyl)-1-(1-phenyl-1H-indazol-5-yl)-propan-1-ol 

Relevant academic research and scientific papers

BTK INHIBITOR

Provided are a series of BTK inhibitors, and specifically disclosed are a compound, pharmaceutically acceptable salt thereof, tautomer thereof or prodrug thereof represented by formula (I), (II), (III) or (IV).

PLANT CIRCADIAN RHYTHM REGULATING AGENT

PROBLEM TO BE SOLVED: To provide a plant circadian rhythm regulating agent, and a more simple and convenient plant circadian rhythm regulating method. SOLUTION: A plant circadian rhythm regulating agent contains a heterocycle-containing compound represented by the general formula (1) or an agriculturally acceptable salt, hydrate or solvate thereof as an active ingredient. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

LIGHT-EMITTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE, ORGANIC ELECTROLUMINESCENT DEVICE USING SAME, AND MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE

Disclosed are a novel fused cyclic compound having excellent light emitting efficiency and thermal stability, a method for producing the same, and an organic electroluminescent device including the same compound. The fused cyclic compound is represented b

Pericyclic rearrangements of N-heterocyclic carbenes of indazole to substituted 9-aminoacridines

On deprotonation, 1-arylindazolium salts form 1-arylindazol-3-ylidenes which rearrange spontaneously via ring cleavage, ring closure and subsequent proton transfer to substituted 9-aminoacridines. By contrast, the N-heterocyclic carbene of 2-phenylindazol