[4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone

Base Information

Chemical Name:[4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone
CAS No.:98795-75-6
Molecular Formula:C21H25NO4
Molecular Weight:355.434
Hs Code.:
ChEMBL ID:CHEMBL5016463
DSSTox Substance ID:DTXSID50539895
Wikidata:Q82415712

Synonyms:98795-75-6;CHEMBL5016463;DTXSID50539895;[4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone

Suppliers and Price of [4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone

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 [4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:355.17835828
Heavy Atom Count:26
Complexity:418

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OCC2=CC=CC=C2)OC)C(=O)N3CCCCC3

Technology Process of [4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone

There total 1 articles about [4-(Benzyloxy)-3,5-dimethoxyphenyl](piperidin-1-yl)methanone 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:

: 110-89-4
piperidine

: 14588-61-5
4-benzyloxy-3,5-dimethoxybenzoic acid chloride

: 98795-75-6
N-(4-Benzyloxy-3,5-dimethoxybenzoyl)piperidine

Guidance literature:: In benzene; Yield given; Heating;
DOI:10.1135/cccc19850510

Reference yield: 90.0%

: 98795-75-6
N-(4-Benzyloxy-3,5-dimethoxybenzoyl)piperidine

: 98795-78-9
N-(4-Hydroxy-3,5-dimethoxybenzoyl)piperidine

Guidance literature:: With hydrogen; pyrographite; palladium dichloride; In ethanol; for 1h; Ambient temperature;
DOI:10.1135/cccc19850510

Reference yield:

: 98795-75-6
N-(4-Benzyloxy-3,5-dimethoxybenzoyl)piperidine

: 98795-81-4
N-<3,5-Dimethoxy-4-(2-dimethylaminoethoxy)benzoyl>piperidine

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / H₂ / PdCl₂, active carbon / ethanol / 1 h / Ambient temperature

2: NaH / dimethylformamide / 5 h / 7 - 10 °C / standing overnight

With hydrogen; sodium hydride; pyrographite; palladium dichloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1135/cccc19850510