3-bromo-N-hydroxybenzamide

Base Information

Chemical Name:3-bromo-N-hydroxybenzamide
CAS No.:2593-28-4
Molecular Formula:C7H6BrNO2
Molecular Weight:216.034
Hs Code.:
ChEMBL ID:CHEMBL2436427
DSSTox Substance ID:DTXSID50567496
Nikkaji Number:J492.578E
Wikidata:Q82453395
Mol file:2593-28-4.mol

Synonyms:3-bromo-N-hydroxybenzamide;2593-28-4;Benzamide, 3-bromo-N-hydroxy-;3-bromobenzohydroxamic acid;CHEMBL2436427;SCHEMBL17336774;3-bromobenzenecarbohydroxamic acid;DTXSID50567496;CAA59328;AKOS000190681;EN300-53712;G19976;Z59181977

Suppliers and Price of 3-bromo-N-hydroxybenzamide

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 7 raw suppliers

Chemical Property of 3-bromo-N-hydroxybenzamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:214.95819
Heavy Atom Count:11
Complexity:151

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Br)C(=O)NO

Technology Process of 3-bromo-N-hydroxybenzamide

There total 6 articles about 3-bromo-N-hydroxybenzamide 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: 87.0%

: 15852-73-0
(3-Bromophenyl)methanol

: 2593-28-4
3-bromo-N-hydroxybenzamide

Guidance literature:: (3-Bromophenyl)methanol; With 1-hydroxy-pyrrolidine-2,5-dione; [bis(acetoxy)iodo]benzene; In acetonitrile; at 0 - 20 ℃; for 3h; Inert atmosphere; Green chemistry;

With hydroxylamine; In water; acetonitrile; for 12h; Inert atmosphere; Green chemistry;
DOI:10.1039/c4ob00693c

Reference yield: 70.0%

: 585-76-2
m-bromobenzoic acid

: 2593-28-4
3-bromo-N-hydroxybenzamide

Guidance literature:: With hydroxylamine hydrochloride; 1,1'-carbonyldiimidazole; In N,N-dimethyl-formamide; for 20h;
DOI:10.1016/j.bmcl.2013.08.081

Reference yield: 50.0%

: 1711-09-7
3-bromobenzoyl chloride

: 2593-28-4
3-bromo-N-hydroxybenzamide

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