70602-99-2

Upstream product

• 15300-12-6 6-morpholino-3,4-dihydro-1(2H)-naphthalenone 
• 50-00-0 formaldehyd 
• 56609-03-1 N-benzhydrylpiperazine hydrochloride 
• 70602-98-1 6-morpholino-3,4-dihydro-1(2H)-naphthalenone hydrochloride 
• 56609-03-1 1-benzhydrylpiperazine hydrochloride 

Downstream Products

• 70603-00-8 2-[(4-benzhydryl-1-piperazinyl)methyl]-6-morpholino-1,2,3,4-tetrahydro-1-naphthalenol 
• 70603-00-8 (1S,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol 
• 70603-00-8 (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol 
• 70603-01-9 4-[6-(4-Benzhydryl-piperazin-1-ylmethyl)-7,8-dihydro-naphthalen-2-yl]-morpholine; hydrochloride 
• 88284-84-8 (1S,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid 
• 88284-84-8 (1R,2S)-2-(4-Benzhydryl-piperazin-1-ylmethyl)-6-morpholin-4-yl-1,2,3,4-tetrahydro-naphthalen-1-ol; compound with (E)-but-2-enedioic acid 

Relevant academic research and scientific papers

Synthesis and biological activities of 3-aminomethyl-1,2-dihydronaphthalene derivatives

A series of 3-aminomethyl-1,2-dihydronaphthalene derivatives was prepared from the corresponding 3,4-dihydro-1(2H)-naphthalenone derivatives in three steps, namely the Mannich reaction, reduction of the carbonyl group with sodium borohydride, and dehydrat

Piperazine containing dihydronaphthalene derivatives and compositions

Novel 1,2-dihydronaphthalene derivatives of the formula STR1 wherein A is a di-lower alkylamino group or a 5- to 7-membered cyclic amino group which may contain one oxygen atom and n is 2 or 3, and its salts have excellent pharmacological activities such