33630-46-5

Upstream product

• 121-33-5 vanillin 
• 143-33-9 sodium cyanide 
• 74-90-8 hydrogen cyanide 
• 151-50-8 potassium cyanide 

Downstream Products

• 115353-19-0 (1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylamino)-(4-hydroxy-3-methoxy-phenyl)-acetonitrile 
• 83530-92-1 α-(benzoylaminomethyl-1,3,4-thiadiazol-2-yl-amino)-(4-hydroxy-3-methoxyphenyl)acetonitrile 
• 83530-82-9 α-(5-o-nitrophenyl-1,3,4-thiadiazol-2-yl-amino)-(4-hydroxy-3-methoxyphenyl)acetonitrile 
• 125237-19-6 p,p'-bis(α-cyano(3-methoxy-4-hydroxyphenyl)methylhydrazinocarbonylmethoxy)diphenyl sulphone 
• 2880-58-2 2-methoxy-1,4-benzoquinone 
• 554-52-9 3-Methoxytyramine 
• 125803-34-1 Acetic acid (R)-cyano-(4-hydroxy-3-methoxy-phenyl)-methyl ester 
• 129313-30-0 Acetic acid (S)-cyano-(4-hydroxy-3-methoxy-phenyl)-methyl ester 

Relevant academic research and scientific papers

Synthesis and antimicrobial activity of some heterocyclic compounds

Condensation of 2-phenyl-3-(4-benzoyl hydride)-1,3-quinazolin-4(4H)-one (1) with various aldehydes gives 2-phenyl-3-(4-arylidene-benzoylhydrazide)-1,3-quinazolin-4(4H)-one (II), which on cycloaddition with mercaptoacetic acid yield 4-thiazolidinones (IIIa-o).Compound (I) on treatment with aromatic cyanohydrines and aryl isothiocyanates gives α-carbohydrazino nitriles of (IVa-m) and thiosemicarbazides (Va-l) respectively.The structures of III-V have been elucidated on the basis of their elemental analysis and spectral data.These compounds exhibit moderate to goodantibacterial and tuberculostatic activities.