Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride)

Base Information

Chemical Name:Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride)
CAS No.:873310-31-7
Molecular Formula:C₁₇H₂₁NO*ClH
Molecular Weight:291.821
Hs Code.:2922199695
Mol file:873310-31-7.mol

Synonyms:Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride);p-Methyl AtoMoxetine Hydrochloride;AtoMoxetine Related CoMpound C;N-Methyl-gamma-(4-methylphenoxy)benzenepropanamine hydrochloride;Atomoxetine EP Impurity C

Suppliers and Price of Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine 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

TRC
p-MethylAtomoxetineHydrochloride
2.5mg
$ 160.00

Total 10 raw suppliers

Chemical Property of Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride)

Chemical Property:

PSA：21.26000
LogP:4.91750

Purity/Quality:

98% ^*data from raw suppliers

p-MethylAtomoxetineHydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Hydrochloride salt of p-Methyl Atomoxetine, impurity of Atomoxetine (A791400), a norepinephrine reuptake inhibitor. p-Methyl Atomoxetine Hydrochloride (Atomoxetine EP Impurity C) is an impurity of Atomoxetine (A791400), a norepinephrine reuptake inhibitor.

Technology Process of Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride)

There total 1 articles about Atomoxetine Related Compound C (10 mg) (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine 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: