33901-47-2

Upstream product

• 108-68-9 3,5-Dimethylphenol 
• 590-17-0 cyanomethyl bromide 

Downstream Products

• 100369-44-6 2-(3,5-dimethyl-phenoxy)-acetimidic acid ethyl ester; hydrochloride 
• 24264-54-8 1-(3,5-Dimethyl-phenoxy)-butan-2-on 
• 26646-46-8 2-(3,5-dimethylphenoxy)ethylamine 
• 111961-63-8 2-(3,5-dimethyl-phenoxy)-acetamidine; hydrochloride 
• 130831-91-3 N,N-diethyl-2-(3,5-dimethyl-phenoxy)-acetamidine; hydrochloride 
• 1443148-08-0 N-[2-(3,5-dimethylphenoxy)ethyl]acetamide 
• 428840-42-0 N-[2-(3,5-dimethylphenoxy)ethyl]-4-nitrobenzamide 
• 316128-77-5 N-[2-(3,5-dimethylphenoxy)ethyl]benzamide 
• 1443148-24-0 methyl (2E)-3-[(2-{2-[methoxy(4-nitrophenyl)methyl]-3,5-dimethylphenoxy}ethyl)(methyl)amino]-acrylate 
• 1443148-23-9 methyl (2E)-3-[(2-{2-[methoxy(phenyl)methyl]-3,5-dimethylphenoxy}ethyl)(methyl)amino]acrylate 
• 1443148-22-8 methyl (2E)-3-[{2-[2-(1-methoxyethyl)-3,5-dimethylphenoxy]ethyl}methylamino]acrylate 
• 1443148-19-3 4,6,8-trimethyl-5-(4-nitrophenyl)-2,3,4,5-tetrahydro-1,4-benzoxazepine 
• 1443148-18-2 4,6,8-trimethyl-5-phenyl-2,3,4,5-tetrahydro-1,4-benzoxazepine 
• 1443148-15-9 4,6,8-trimethyl-5-(4-nitrophenyl)-2,3-dihydro-1,4-benzoxazepinium iodide 

Relevant academic research and scientific papers

Transformations of tetrahydro-1,4-benzoxazepines and tetrahydro-1,4- benzothiazepines under the action of alkynes. First example of the synthesis of tetrahydro-1,4-benzothiazonine-6-carboxylate

It was shown that 2,3,4,5-tetrahydro-1,4-benzoxazepines were cleaved at the N-C(5) bond under the action of activated alkynes in methanol, forming o-(methoxyethyl)- and o-(methoxybenzyl)-phenyl(aminoethyl) ethers. The cleavage rate depended on the electro