73628-00-9

Upstream product

• 67-56-1 methanol 
• 95-14-7 1,2,3-Benzotriazole 
• 100-52-7 benzaldehyde 
• 1125-88-8 benzaldehyde dimethyl acetal 

Downstream Products

• 7203-48-7 (1R*,3R*)-3-ethoxy-1-methoxy-1,3-diphenylpropane 
• 7203-48-7 (1R*,3S*)-3-ethoxy-1-methoxy-1,3-diphenylpropane 
• 143064-61-3 3-ethoxy-1-methoxy-1-phenylpropane 
• 202396-13-2 1-(1-Ethyl-3-methoxy-1-phenoxy-3-phenyl-propyl)-1H-benzotriazole 
• 110743-59-4 1-phenyloctane-1,6-dione 
• 223128-83-4 1-(benzotriazol-1-yl)-5-bromo-1-methoxy-1-phenylpentane 
• 3375-38-0 1,4-dibenzoylbutane 
• 53395-25-8 1,1'-(3-methoxyprop-1-yne-1,3-diyl)dibenzene 
• 202396-08-5 1-(3-Methoxy-1-phenoxy-3-phenyl-propyl)-1H-benzotriazole 
• 202396-06-3 1-(benzotriazol-1-yl)ethyl phenyl ether 
• 95-14-7 1,2,3-Benzotriazole 
• 100-52-7 benzaldehyde 
• 300683-29-8 3-(benzotriazol-1-yl)-3-ethoxy-1-methoxy-1-phenylpropane 
• 143064-64-6 (1R*,2S*,3R*)-3-(benzotriazol-1-yl)-1,2-diphenyl-1,3-dimethoxypropane 

Relevant academic research and scientific papers

The Chemistry of N-Substituted Benzotriazoles. Part 2. Reactions of Benzotriazole with Aldehydes and Aldehyde Derivatives. 1-(α-Hydroxyalky)-, 1-(α-Alkoxyalkyl)-, and 1-(α-Acyloxyalkyl)benzotriazoles

Benzotriazole reacts readily with a variety of aldehydes to yield crystalline 1:1 adducts characterized by strong hydrogen bonding.Corresponding 1-(α-alkoxyalkyl)benzotriazoles are formed in the presence of alcohols, and 1-(α-acetoxyalkyl) analogues resul

REACTIVITY OF AZOLES TOWARDS BENZALDEHYDE AND ITS DIMETHYLACETAL. SYNTHESIS OF N,N'-DIAZOLYLPHENYLMETHANES

Some 1,1'-diindazolylphenylmethanes have been prepared from indazoles and benzaldehyde in presence of zinc chloride as catalyst.The reaction was strongly dependent on the basic pKa's of azoles and only few pyrazolyl derivatives could be prepare