N-butyl-3,4,5-trihydroxybenzamide

Base Information

Chemical Name:N-butyl-3,4,5-trihydroxybenzamide
CAS No.:110482-92-3
Molecular Formula:C11H15NO4
Molecular Weight:225.244
Hs Code.:
DSSTox Substance ID:DTXSID40546694
Wikidata:Q82424596
Mol file:110482-92-3.mol

Synonyms:N-butyl-3,4,5-trihydroxybenzamide;110482-92-3;SCHEMBL15069976;DTXSID40546694;RPXISHBMAMYFNI-UHFFFAOYSA-N

Suppliers and Price of N-butyl-3,4,5-trihydroxybenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-butyl-3,4,5-trihydroxybenzamide

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:225.10010796
Heavy Atom Count:16
Complexity:222

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCNC(=O)C1=CC(=C(C(=C1)O)O)O

Technology Process of N-butyl-3,4,5-trihydroxybenzamide

There total 7 articles about N-butyl-3,4,5-trihydroxybenzamide 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: 60.0%

: 149-91-7
3,4,5-trihydroxybenzoic acid

: 109-73-9,85404-21-3
N-butylamine

: 110482-92-3
3,4,5-trihydroxy-N-butyl-benzamide

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.13005/ojc/340323

Reference yield: 51.0%

: 1416324-89-4
3,4,5-tris(benzyloxy)-N-butylbenzamide

: 110482-92-3
3,4,5-trihydroxy-N-butyl-benzamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 13 ℃; for 20h;
DOI:10.1002/anie.201204910