4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride

Base Information

Chemical Name:4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride
CAS No.:875126-51-5
Molecular Formula:C₁₃H₂₀N₂*2ClH
Molecular Weight:277.237
Hs Code.:
Mol file:875126-51-5.mol

Synonyms:Benzenemethanamine,4-(1-piperidinylmethyl)-, dihydrochloride (9CI);[4-[(Piperidin-1-yl)methyl]benzyl]aminedihydrochloride;

Suppliers and Price of 4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride

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
4-(1-PIPERIDINYLMETHYL)-BENZENEMETHANAMINE DIHYDROCHLORIDE 95.00%
5MG
$ 501.80

Total 5 raw suppliers

Chemical Property of 4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride

Chemical Property:

PSA：29.26000
LogP:4.37340

Purity/Quality:

99% ^*data from raw suppliers

4-(1-PIPERIDINYLMETHYL)-BENZENEMETHANAMINE DIHYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride

There total 3 articles about 4-(1-Piperidinylmethyl)-benzenemethanaminedihydrochloride 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: 99.0%

: (4-piperidin-1-ylmethyl-benzyl)-carbamic acid tert-butyl ester

: 875126-51-5
4-piperidin-1-ylmethyl-benzylamine dihydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; methanol; at 20 ℃; for 2.5h;
DOI:10.1021/jm061224g

Reference yield:

: 111-24-0
1,5-dibromo-pentane

: 875126-51-5
4-piperidin-1-ylmethyl-benzylamine dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 26 percent / K₂CO₃ / acetonitrile / Heating

2: 99 percent / HCl / methanol; dioxane / 2.5 h / 20 °C

With hydrogenchloride; potassium carbonate; In 1,4-dioxane; methanol; acetonitrile;
DOI:10.1021/jm061224g

Reference yield:

: 108468-00-4
tert-butyl 4-(aminomethyl)benzylcarbamate

: 875126-51-5
4-piperidin-1-ylmethyl-benzylamine dihydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 26 percent / K₂CO₃ / acetonitrile / Heating

2: 99 percent / HCl / methanol; dioxane / 2.5 h / 20 °C

With hydrogenchloride; potassium carbonate; In 1,4-dioxane; methanol; acetonitrile;
DOI:10.1021/jm061224g