N,3,5-trihydroxybenzamide

Base Information

Chemical Name:N,3,5-trihydroxybenzamide
CAS No.:30697-84-8
Molecular Formula:C7H7 N O4
Molecular Weight:169.137
Hs Code.:2924299090
ChEMBL ID:CHEMBL389593
DSSTox Substance ID:DTXSID20574591
Wikidata:Q82463697
Mol file:30697-84-8.mol

Synonyms:N,3,5-trihydroxybenzamide;30697-84-8;3,5-DIHYDROXYBENZOHYDROXAMIC ACID;CHEMBL389593;Benzamide, N,3,5-trihydroxy-;SCHEMBL10530665;DTXSID20574591;AKOS006292707

Suppliers and Price of N,3,5-trihydroxybenzamide

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
3,5-DIHYDROXYBENZOHYDROXAMIC ACID 95.00%
5MG
$ 501.80

Total 4 raw suppliers

Chemical Property of N,3,5-trihydroxybenzamide

Chemical Property:

PSA：89.79000
LogP:0.60770
XLogP3:0
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:169.03750770
Heavy Atom Count:12
Complexity:163

Purity/Quality:

99% ^*data from raw suppliers

3,5-DIHYDROXYBENZOHYDROXAMIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C=C(C=C1O)O)C(=O)NO

Technology Process of N,3,5-trihydroxybenzamide

There total 6 articles about N,3,5-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: 84.0%

: 932380-56-8
N-(benzyloxy)-3,5-dihydroxybenzamide

: 30697-84-8
3,5-dihydroxybenzohydroxamic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 23 ℃; for 0.5h;
DOI:10.1016/j.bmcl.2006.11.053

Reference yield:

: 28917-43-3
3,5-dibenzyloxybenzoic acid

: 30697-84-8
3,5-dihydroxybenzohydroxamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 4-methyl-morpholine / diethyl ether

2: hydroxylamine hydrochloride / methanol

3: palladium 10% on activated carbon; hydrogen / methanol

With 4-methyl-morpholine; palladium 10% on activated carbon; hydroxylamine hydrochloride; hydrogen; In methanol; diethyl ether;
DOI:10.1039/c5ra25256c

Reference yield:

: C₂₄H₂₂O₆

: 30697-84-8
3,5-dihydroxybenzohydroxamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride / methanol

2: palladium 10% on activated carbon; hydrogen / methanol

With palladium 10% on activated carbon; hydroxylamine hydrochloride; hydrogen; In methanol;
DOI:10.1039/c5ra25256c