122483-88-9

Upstream product

• 104-54-1 3-Phenylpropenol 
• 608-25-3 2-methylbenzene-1,3-diol 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 

Downstream Products

• 127055-92-9 6,7-dihydro-10-methyl-8-phenyl-2H,8H-benzo<1,2-b:5,4-b'>dipyran-2-one 
• 127055-96-3 6,7-dihydro-4,10-dimethyl-8-phenyl-2H,8H-benzo<1,2-b:5,4-b'>dipyran-2-one 
• 127055-99-6 6,7-dihydro-10-methyl-4,8-diphenyl-2H,8H-benzo<1,2-b:5,4-b'>dipyran-2-one 
• 122483-90-3 ethyl (3,4-dihydro-8-methyl-2-phenyl-2H-1-benzopyran-7-yloxy)acetate 
• 122483-92-5 3,4-dihydro-8-methyl-2-phenyl-2H-1-benzopyran-7-yloxyacetic acid hydrazide 
• 122484-26-8 5-(3',4'-dihydro-8'-methyl-2'-phenyl-2'H-1'-benzopyran-7'-yloxymethyl)-2-mercapto-1,3,4-oxadiazole 
• 122484-32-6 N-benzylidene-3,4-dihydro-8-methyl-2-phenyl-2H-1-benzopyran-7-yloxyacetic acid hydrazide 
• 122484-33-7 (8-Methyl-2-phenyl-chroman-7-yloxy)-acetic acid [1-p-tolyl-meth-(E)-ylidene]-hydrazide 
• 122484-34-8 (8-Methyl-2-phenyl-chroman-7-yloxy)-acetic acid [1-(4-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 122484-17-7 5-(3',4'-dihydro-8'-methyl-2'-phenyl-2'H-1'-benzopyran-7'-yloxymethyl)-4-phenyl-1,2,4-triazole-3(4H)-thiol 
• 122484-21-3 5-(8-Methyl-2-phenyl-chroman-7-yloxymethyl)-4-o-tolyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 122484-22-4 5-(8-Methyl-2-phenyl-chroman-7-yloxymethyl)-4-m-tolyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 122484-23-5 5-(8-Methyl-2-phenyl-chroman-7-yloxymethyl)-4-p-tolyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 122484-35-9 (8-Methyl-2-phenyl-chroman-7-yloxy)-acetic acid [1-(3,4-dimethoxy-phenyl)-meth-(E)-ylidene]-hydrazide 

Relevant academic research and scientific papers

CARBAZOLE CARBOXAMIDE COMPOUNDS USEFUL AS KINASE INHIBITORS

Compounds having the formula (I), and enantiomers, and diastereomers, pharmaceutically-acceptable salts, thereof, are useful as kinase modulators, including Btk modulation.

Acid-catalysed Condensation of Phenolic Compounds with Cinnamyl Alcohol. Synthesis of Flavans and Linear Pyranocoumarins

Acid-catalysed condensation of 2-methylresorcinol (1) with cinnamyl alcohol gave 2-4.The flavan (3) has been used for the synthesis of dihydropyranocoumarins (5, 10 and 14) which on dehydrogenation with DDQ gave the pyranocoumarins (8, 12 and 15, respecti