o-Carboxybenzhydroxamic acid

Base Information

Chemical Name:o-Carboxybenzhydroxamic acid
CAS No.:17698-09-8
Molecular Formula:C8H7NO4
Molecular Weight:181.148
Hs Code.:
NSC Number:524748
UNII:39GC6SA6FX
DSSTox Substance ID:DTXSID00170232
Nikkaji Number:J1.903.653G
Wikidata:Q83040125

Synonyms:o-Carboxybenzhydroxamic acid;Phthalmonohydroxamic acid;o-Carboxybenzohydroxamic acid;17698-09-8;Phthalamic acid, N-hydroxy-;Phthalomonohydroxamic acid;2-Carboxybenzohydroxamic acid;39GC6SA6FX;NSC-524748;Benzoic acid, 2-((hydroxyamino)carbonyl)-;Benzoic acid, 2-[(hydroxyamino)carbonyl]-;2-(hydroxycarbamoyl)benzoic acid;NSC 524748;N-hydroxyphthalamic acid;UNII-39GC6SA6FX;Benzoic acid, 2-((hydroxyamino)carbonyl)- (9CI);SCHEMBL1026322;DTXSID00170232;NSC524748;2-((HYDROXYAMINO)CARBONYL)BENZOIC ACID

Suppliers and Price of o-Carboxybenzhydroxamic acid

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 5 raw suppliers

Chemical Property of o-Carboxybenzhydroxamic acid

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.469g/cm³
XLogP3:0
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:181.03750770
Heavy Atom Count:13
Complexity:216

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of o-Carboxybenzhydroxamic acid

There total 8 articles about o-Carboxybenzhydroxamic acid 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: 98.0%

: 85-44-9
phthalic anhydride

: 17698-09-8
2-[(hydroxyamino)carbonyl]benzoic acid

Guidance literature:: With hydroxylamine hydrochloride; sodium hydroxide; In water; at 20 ℃; for 2h; Inert atmosphere; Cooling with ice;

Reference yield: 12.0%

: 77-36-1
chlorthalidon

: 2224-77-3
3-(4'-chlorophenyl)-1-isoindolinone

: 17698-09-8
2-[(hydroxyamino)carbonyl]benzoic acid

: 835-18-7
3-phenyl-2,3-dihydro-isoindol-1-one

Guidance literature:: With oxygen; In methanol; at 20 ℃; for 72h; Further Variations:; Reagents; sensitizers and scavengers; Product distribution; Quantum yield; UV-irradiation;