1-(2-Methylbenzyl)piperazine hydrochloride

Base Information

Chemical Name:1-(2-Methylbenzyl)piperazine hydrochloride
CAS No.:5321-51-7
Molecular Formula:C₁₂H₁₈N₂*ClH
Molecular Weight:226.749
Hs Code.:
ChEMBL ID:CHEMBL1504319

Synonyms:1-(2-Methylbenzyl)piperazine hydrochloride;435345-16-7;1-(2-Methyl-benzyl)-piperazine hydrochloride;1-[(2-Methylphenyl)Methyl]Piperazine Hydrochloride;1-[(2-methylphenyl)methyl]piperazine;hydrochloride;1-(2-Methyl-benzyl)-piperazinehydrochloride;MLS000856063;SCHEMBL2924720;CHEMBL1504319;1-(2-Methyl-benzyl)-piperazine;AKOS015844170;SMR000282808;CS-0357680

Suppliers and Price of 1-(2-Methylbenzyl)piperazine hydrochloride

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

ChemBridge Corporation
1-(2-methylbenzyl)piperazinedihydrochloride 95%
1 g
$ 23.00

American Custom Chemicals Corporation
1-(2-METHYL-BENZYL)PIPERAZINE DIHYDROCHLORIDE 98.00%
5MG
$ 496.90

Total 5 raw suppliers

Chemical Property of 1-(2-Methylbenzyl)piperazine hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:226.1236763
Heavy Atom Count:15
Complexity:164

Purity/Quality:

99% ^*data from raw suppliers

1-(2-methylbenzyl)piperazinedihydrochloride 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=CC=C1CN2CCNCC2.Cl

Technology Process of 1-(2-Methylbenzyl)piperazine hydrochloride

There total 1 articles about 1-(2-Methylbenzyl)piperazine hydrochloride 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: