N-hydroxy-3,5-dimethoxybenzamide

Base Information

Chemical Name:N-hydroxy-3,5-dimethoxybenzamide
CAS No.:710311-79-8
Molecular Formula:C9H11 N O4
Molecular Weight:197.191
Hs Code.:
DSSTox Substance ID:DTXSID70408711
Wikidata:Q82214286
Mol file:710311-79-8.mol

Synonyms:N-hydroxy-3,5-dimethoxybenzamide;710311-79-8;SCHEMBL6465455;DTXSID70408711;AKOS000187236

Suppliers and Price of N-hydroxy-3,5-dimethoxybenzamide

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 1 raw suppliers

Chemical Property of N-hydroxy-3,5-dimethoxybenzamide

Chemical Property:

Melting Point:141-143 °C
PKA:8.38±0.10(Predicted)
PSA：71.28000
Density:1.241±0.06 g/cm3(Predicted)
LogP:1.39760
XLogP3:0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:197.06880783
Heavy Atom Count:14
Complexity:185

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1)C(=O)NO)OC

Technology Process of N-hydroxy-3,5-dimethoxybenzamide

There total 3 articles about N-hydroxy-3,5-dimethoxybenzamide 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: 78.0%

: 17213-57-9
3,5-dimethoxybenzoyl chloride

: 710311-79-8
N-hydroxy-3,5-dimethoxybenzamide

Guidance literature:: With hydroxylamine hydrochloride; potassium carbonate; In water; ethyl acetate; at 0 - 20 ℃; for 16h;
DOI:10.1039/c8ob00490k

Reference yield:

: 1132-21-4
3,5-dimethoxybenzoic acid

: 710311-79-8
N-hydroxy-3,5-dimethoxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 1 h / 20 °C

2: hydroxylamine / acetonitrile; water / 14 h / 23 °C

With hydroxylamine; In water; acetonitrile;
DOI:10.1021/ol303424b