Ropizine

Base Information

Chemical Name:Ropizine
CAS No.:3601-19-2
Molecular Formula:C24H26 N4
Molecular Weight:370.497
Hs Code.:
NSC Number:300584
UNII:Q5128GW9D4
DSSTox Substance ID:DTXSID60189567
NCI Thesaurus Code:C75166
ChEMBL ID:CHEMBL2107093
Mol file:3601-19-2.mol

Synonyms:1-benzhydryl-4-(6-methyl-2-pyridylmethyleneimino)piperazine;ropizine;SC-13504

Suppliers and Price of Ropizine

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

American Custom Chemicals Corporation
N-(4-BENZHYDRYL-1-PIPERAZINYL)-N-[(E)-(6-METHYL-2-PYRIDINYL)METHYLIDENE]AMINE 95.00%
5MG
$ 505.40

Total 7 raw suppliers

Chemical Property of Ropizine

Chemical Property:

Vapor Pressure:2.16E-11mmHg at 25°C
Melting Point:105-107 °C
Boiling Point:531.8°Cat760mmHg
PKA:6.69±0.10(Predicted)
Flash Point:275.4°C
PSA：31.73000
Density:1.1g/cm³
LogP:4.00690
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:370.21574685
Heavy Atom Count:28
Complexity:455

Purity/Quality:

99% ^*data from raw suppliers

N-(4-BENZHYDRYL-1-PIPERAZINYL)-N-[(E)-(6-METHYL-2-PYRIDINYL)METHYLIDENE]AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC(=CC=C1)C=NN2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4
Isomeric SMILES:CC1=NC(=CC=C1)/C=N/N2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4
Uses Anticonvulsant. Ropazine acts as an anticonvulsant agent and often in tandem with dextromethorphan.

Technology Process of Ropizine

There total 3 articles about Ropizine 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: