Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-

Base Information

Chemical Name:Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-
CAS No.:83823-35-2
Molecular Formula:C₂₁H₂₄N₂O₂
Molecular Weight:336.434
Hs Code.:
DSSTox Substance ID:DTXSID60232729
Wikidata:Q83113843

Synonyms:BRN 4567586;Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-;1-(2H-1-Benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)piperazine;83823-35-2;DTXSID60232729;LS-110335

Suppliers and Price of Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-

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 Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-

Chemical Property:

Vapor Pressure:7.53E-10mmHg at 25°C
Boiling Point:492.7°Cat760mmHg
Flash Point:143.4°C
Density:1.164g/cm³
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:336.183778013
Heavy Atom Count:25
Complexity:459

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC=C1N2CCN(CC2)CC3=CC4=CC=CC=C4OC3

Technology Process of Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)-

There total 6 articles about Piperazine, 1-(2H-1-benzopyran-3-ylmethyl)-4-(2-methoxyphenyl)- 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:

: 90-02-8
salicylaldehyde

: 83823-35-2
1-(2H-Chromen-3-ylmethyl)-4-(2-methoxy-phenyl)-piperazine

Guidance literature:: Multi-step reaction with 5 steps

1: 16 percent / 20percent aq.NaOH

2: 94.7 percent / 10percent NaOH / 5 h / Heating

3: SOCl₂ / benzene / 3 h / Heating

4: Et₃N / benzene

5: LiAlH₄ / diethyl ether / Heating

With sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; triethylamine; In diethyl ether; benzene;

Reference yield:

: 83823-27-2
(2H-Chromen-3-yl)-[4-(2-methoxy-phenyl)-piperazin-1-yl]-methanone

: 83823-35-2
1-(2H-Chromen-3-ylmethyl)-4-(2-methoxy-phenyl)-piperazine

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; Heating;

Reference yield:

: 57543-66-5
2H-chromene-3-carbonitrile

: 83823-35-2
1-(2H-Chromen-3-ylmethyl)-4-(2-methoxy-phenyl)-piperazine

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / 10percent NaOH / Heating

2: SOCl₂ / benzene / 3 h / Heating

3: Et₃N / benzene

4: LiAlH₄ / diethyl ether / Heating

With sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; triethylamine; In diethyl ether; benzene;