1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine

Base Information

Chemical Name:1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine
CAS No.:88285-49-8
Molecular Formula:C₂₉H₃₀N₂O
Molecular Weight:422.57
Hs Code.:
DSSTox Substance ID:DTXSID70525058
Wikidata:Q82392376

Synonyms:88285-49-8;DTXSID70525058;1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine

Suppliers and Price of 1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine

Chemical Property:

XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:422.235813585
Heavy Atom Count:32
Complexity:529

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)C=C(C=C2)CN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=CC=C5

Technology Process of 1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine

There total 5 articles about 1-(Diphenylmethyl)-4-[(6-methoxynaphthalen-2-yl)methyl]piperazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 2471-70-7
2-methoxy-6-naphthoic acid

: 88285-49-8
1-benzhydryl-4-(6-methoxy-2-naphthyl)methylpiperazine

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / 10percent HCl / 6 h / Heating

2: 86 percent / LiAlH₄ / diethyl ether / 1 h / Ambient temperature

3: SOCl₂, pyridine / CHCl₃ / 0.5 h / Ambient temperature

4: K₂CO₃ / acetone / 6 h / Heating

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; In diethyl ether; chloroform; acetone;
DOI:10.1248/cpb.31.2006

Reference yield:

: 60201-22-1
(6-methoxy-2-naphthyl)methanol

: 88285-49-8
1-benzhydryl-4-(6-methoxy-2-naphthyl)methylpiperazine

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂, pyridine / CHCl₃ / 0.5 h / Ambient temperature

2: K₂CO₃ / acetone / 6 h / Heating

With pyridine; thionyl chloride; potassium carbonate; In chloroform; acetone;
DOI:10.1248/cpb.31.2006

Reference yield:

: 78112-30-8
6-methoxy-3,4-dihydronaphthalene-2-carboxylic acid

: 88285-49-8
1-benzhydryl-4-(6-methoxy-2-naphthyl)methylpiperazine

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / sulfur / 0.5 h / 220 - 230 °C

2: 91 percent / 10percent HCl / 6 h / Heating

3: 86 percent / LiAlH₄ / diethyl ether / 1 h / Ambient temperature

4: SOCl₂, pyridine / CHCl₃ / 0.5 h / Ambient temperature

5: K₂CO₃ / acetone / 6 h / Heating

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; sulfur; In diethyl ether; chloroform; acetone;
DOI:10.1248/cpb.31.2006