4-Hydroxybenzohydroxamic acid

Base Information

• Chemical Name: 4-Hydroxybenzohydroxamic acid
• CAS No.: 5941-13-9
• Molecular Formula: C7H7NO3
• Molecular Weight: 153.137
• Hs Code.: 2924299090
• European Community (EC) Number: 653-166-7
• NSC Number: 111680
• DSSTox Substance ID: DTXSID10974824
• Nikkaji Number: J275.025B
• Wikidata: Q82959279
• ChEMBL ID: CHEMBL158240
• Mol file: 5941-13-9.mol

Synonyms:N,4-dihydroxybenzamide;5941-13-9;4-Hydroxybenzohydroxamic acid;4,N-Dihydroxy-benzamide;p-Hydroxybenzohydroxamic acid;CHEMBL158240;1-N-hydroxy4-hydroxybenzene-1-carboximidic acid;Benzamide, N,4-dihydroxy-;Benzohydroxamic acid, p-hydroxy-;4,N-dihydroxybenzamide;n,4-Dihydroxy-benzamide;SCHEMBL1151494;3-Chlorobiphenyl-2-carbaldehyde;DTXSID10974824;BDBM50015098;N,4-dihydroxybenzenecarboximidic acid;NSC111680;AKOS000177673;AKOS024334007;NSC-111680;CS-0257044;FT-0693056;EN300-658995

Chemical Property of 4-Hydroxybenzohydroxamic acid

Chemical Property:

• Vapor Pressure: 7.23E-20mmHg at 25°C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 69.56000
• Density: 1.402g/cm³
• LogP: 0.90210
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 153.042593085
• Heavy Atom Count: 11
• Complexity: 141

Purity/Quality:

97% ^*data from raw suppliers

4,N-DIHYDROXY-BENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C(=O)NO)O

Technology Process of 4-Hydroxybenzohydroxamic acid

There total 9 articles about 4-Hydroxybenzohydroxamic 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: 99.0%

N-(benzyloxy)-4-hydroxybenzamide (732308-76-8) → 4-hydroxyphenylhydroxamic acid (5941-13-9)

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: 21.0%

methyl 4-hydroxylbenzoate (99-76-3,156291-94-0) → 4-hydroxyphenylhydroxamic acid (5941-13-9)

Guidance literature:

With hydroxylamine hydrochloride; sodium hydroxide; In water; at 20 ℃; for 4h;

DOI:10.1039/c9sc02557j

Reference yield: 10.0%

4-hydroxy-N-((tetrahydro-2H-pyran-2-yl)oxy)benzamide → 4-hydroxyphenylhydroxamic acid (5941-13-9)

Guidance literature:

With hydrogenchloride; In water; acetonitrile; at 20 ℃; for 4h; Inert atmosphere;

DOI:10.1007/s12272-018-1045-z

upstream raw materials:

methyl 4-hydroxylbenzoate

N-(benzyloxy)-4-hydroxybenzamide

C₁₄H₁₃NO₃

p-(benzyloxy)benzoic acid

Downstream raw materials:

[Fe(4-hydroxybenzoic hydroxamate)₃]

oxo hydroxo bis-(4-hydroxy benzhydroxamato) vanadium (V)

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