Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-

Base Information

Chemical Name:Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-
CAS No.:192802-99-6
Molecular Formula:C25H28N2O3
Molecular Weight:404.509
Hs Code.:
DSSTox Substance ID:DTXSID50471968
Wikidata:Q82300686

Synonyms:Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-;192802-99-6;SCHEMBL21023149;DTXSID50471968

Suppliers and Price of Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:404.20999276
Heavy Atom Count:30
Complexity:475

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC=CC(=C2OCC3=CC=CC=C3)C(=O)NCCCCN

Technology Process of Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)-

There total 7 articles about Benzamide, N-(4-aminobutyl)-2,3-bis(phenylmethoxy)- 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%

: N-(aminobutyl)-2,3-bis(benzyloxy)benzamide trifluoroacetate

: 192802-99-6
N-(aminobutyl)-2,3-bis(benzyloxy)benzamide

Guidance literature:: With sodium hydroxide; In water; at 20 ℃; for 0.5h;
DOI:10.1039/d0dt00689k

Reference yield:

: 74272-78-9
2,3-dibenzyloxybenzoic acid

: 192802-99-6
N-(aminobutyl)-2,3-bis(benzyloxy)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / dichloromethane / 0.5 h

1.2: 20 °C

2.1: dichloromethane / 3 h / 0 - 20 °C

3.1: sodium hydroxide / water / 0.33 h

With benzotriazol-1-ol; dicyclohexyl-carbodiimide; sodium hydroxide; In dichloromethane; water;
DOI:10.1016/j.poly.2016.09.006

Reference yield:

: N-(N’-tert-butyloxycarbonylbutanediamino)-2,3-bis(benzyloxy)benzamide

: 192802-99-6
N-(aminobutyl)-2,3-bis(benzyloxy)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 3 h / 0 - 20 °C

2: sodium hydroxide / water / 0.33 h

With sodium hydroxide; In dichloromethane; water;
DOI:10.1016/j.poly.2016.09.006