Dibenzhydroxamic acid

Base Information

• Chemical Name: Dibenzhydroxamic acid
• CAS No.: 959-32-0
• Molecular Formula: C14H11NO3
• Molecular Weight: 241.246
• Hs Code.: 2924299090
• NSC Number: 405532,25420,5998
• UNII: N1LIW08DJR
• DSSTox Substance ID: DTXSID20242021
• Nikkaji Number: J86.776D
• Wikidata: Q83125615
• ChEMBL ID: CHEMBL1520812
• Mol file: 959-32-0.mol

Synonyms:Dibenzhydroxamic acid;benzamido benzoate;N,O-Dibenzoylhydroxylamine;Dibenzohydroxamic acid;Benzamide, N-(benzoyloxy)-;959-32-0;Hydroxylamine, N,O-dibenzoyl-;N-(benzoyloxy)benzamide;O-Benzoyl benzohydroxamate;NSC 5998;NSC 25420;N1LIW08DJR;NSC 405532;BRN 1880381;AI3-15872;NSC-5998;NSC-25420;NSC-405532;Hydroxylamine,O-dibenzoyl-;4-09-00-00914 (Beilstein Handbook Reference);(Benzoylamino)benzoate;Bio1G10;UNII-N1LIW08DJR;MLS000851104;SCHEMBL5809526;CHEMBL1520812;SCHEMBL11208435;DTXSID20242021;NSC5998;HMS1661B11;HMS2812A15;NSC25420;O-BENZOYLBENZOHYDROXAMIC ACID;CCG-54435;NSC405532;O-BENZOYLBENZENEHYDROXAMIC ACID;BENZOIC ACID, BENZOYLAZANYL ESTER;NCGC00246662-01;LS-77404;SMR000457347;SR-01000643530-1;BRD-K85449954-001-09-9

Chemical Property of Dibenzhydroxamic acid

Chemical Property:

• PSA: 55.40000
• Density: 1.233g/cm³
• LogP: 2.57930
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 241.07389321
• Heavy Atom Count: 18
• Complexity: 291

Purity/Quality:

99% ^*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)NOC(=O)C2=CC=CC=C2

Technology Process of Dibenzhydroxamic acid

There total 76 articles about Dibenzhydroxamic 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: 17.0%

Benzohydroxamic acid (495-18-1) → N-(benzoyloxy)benzamide (959-32-0) + benzoic acid anhydride (93-97-0)

Guidance literature:

With tetraethylammonium metaperiodate; In dichloromethane; at 0 ℃; for 1h;

Reference yield:

hydrogenchloride (7647-01-0,15364-23-5) + (N-benzoyloxy-benzimidic acid )-(4-methoxy-benzoic acid )-anhydride (153797-47-8) → N-(benzoyloxy)benzamide (959-32-0) + 4-methoxybenzoic acid (100-09-4)

Guidance literature:

α-form;

Reference yield:

benzoic acid-[N-(4-methoxy-benzoyloxy)-benzimidic acid ]-anhydride → N-(benzoyloxy)benzamide (959-32-0) + N-benzoyl-O-(4-methoxy-benzoyl)-hydroxylamine (59101-33-6) + 4-methoxybenzoic acid (100-09-4) + benzoic acid (65-85-0,8013-63-6)

Guidance literature:

α-form;

upstream raw materials:

pyridine

N-hydroxyurea

benzoyl chloride

1-nitro-1-phenylmethane

Downstream raw materials:

Benzohydroxamic acid

benzoic acid

N-phenyl benzoyl amide

N-benzoyl-N'-phenylhydrazine