N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl

Base Information

Chemical Name:N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl
CAS No.:125575-13-5
Molecular Formula:C24H32 N4 O3 . Cl H
Molecular Weight:460.9968
Hs Code.:
DSSTox Substance ID:DTXSID40154798
Mol file:125575-13-5.mol

Synonyms:N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl;125575-13-5;Benzenecarboximidamide, N-(2-(4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxy-,monohydrochloride;C24H32N4O3.ClH;DTXSID40154798;C24-H32-N4-O3.Cl-H;LS-29404

Suppliers and Price of N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl

Chemical Property:

Boiling Point:579°Cat760mmHg
Flash Point:304°C
Density:g/cm³
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:460.2241186
Heavy Atom Count:32
Complexity:559

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCOC1=CC=C(C=C1)C(=NCCN2CCN(CC2)CC3=CC4=C(C=C3)OCO4)N.Cl

Technology Process of N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl

There total 6 articles about N-(2-(4-(1,3-Benzodioxol-5-ylmethyl)-1-piperazinyl)ethyl)-4-propoxybenzenecarboximidamide HCl 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: 90.0%

: C₁₀H₁₄N₂O*ClH*H₂O

: 24220-86-8
<(methylenedioxy-3,4 benzyl)-4 piperazinyl>-2 ethylamine

: 125575-13-5
N-[2-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-1-yl)-ethyl]-4-propoxy-benzamidine; hydrochloride

Guidance literature:: In ethanol; Heating;
DOI:10.1016/0223-5234(89)90088-3

Reference yield:

: 32231-06-4
1-Piperonylpiperazine

: 125575-13-5
N-[2-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-1-yl)-ethyl]-4-propoxy-benzamidine; hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / toluene / 3 h / Heating

2: 72 percent / H₂, NH₃ / Raney-Ni / ethanol / 6 h / 70 °C / 90007.2 Torr

3: 90 percent / ethanol / Heating

With ammonia; hydrogen; nickel; In ethanol; toluene;
DOI:10.1016/0223-5234(89)90088-3

Reference yield:

: 125575-24-8
<(methylenedioxy-3,4 benzyl)-4 piperazinyl>-acetonitrile

: 125575-13-5
N-[2-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-1-yl)-ethyl]-4-propoxy-benzamidine; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / H₂, NH₃ / Raney-Ni / ethanol / 6 h / 70 °C / 90007.2 Torr

2: 90 percent / ethanol / Heating

With ammonia; hydrogen; nickel; In ethanol;
DOI:10.1016/0223-5234(89)90088-3