Acetohydroxamic acid, N-fluoren-1-YL-

Base Information

Chemical Name:Acetohydroxamic acid, N-fluoren-1-YL-
CAS No.:22251-01-0
Molecular Formula:C₁₅H₁₃NO₂
Molecular Weight:239.274
Hs Code.:2924299090
DSSTox Substance ID:DTXSID80176792
Nikkaji Number:J33.475H
Wikidata:Q83047089
ChEMBL ID:CHEMBL280245
Mol file:22251-01-0.mol

Synonyms:1-Fluorenylacethydroxamic acid;22251-01-0;N-Fluoren-1-ylacetohydroxamic acid;ACETOHYDROXAMIC ACID, N-FLUOREN-1-YL-;N-Hydroxy-1-fluorenylacetamide;BRN 2131585;CHEMBL280245;DTXSID80176792;N-(9H-Fluoren-1-yl)acetohydroxamic acid;Acetamide, N-9H-fluoren-1-yl-N-hydroxy-

Suppliers and Price of Acetohydroxamic acid, N-fluoren-1-YL-

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

American Custom Chemicals Corporation
N-FLUOREN-1-YL-ACETOHYDROXAMIC ACID 95.00%
5MG
$ 503.59

Total 5 raw suppliers

Chemical Property of Acetohydroxamic acid, N-fluoren-1-YL-

Chemical Property:

Vapor Pressure:2.82E-08mmHg at 25°C
Melting Point:79°C
Refractive Index:1.5500 (estimate)
Boiling Point:433.3°Cat760mmHg
Flash Point:215.9°C
PSA：40.54000
Density:1.322g/cm³
LogP:2.99990
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:239.094628657
Heavy Atom Count:18
Complexity:331

Purity/Quality:

99% ^*data from raw suppliers

N-FLUOREN-1-YL-ACETOHYDROXAMIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N(C1=CC=CC2=C1CC3=CC=CC=C32)O

Technology Process of Acetohydroxamic acid, N-fluoren-1-YL-

There total 5 articles about Acetohydroxamic acid, N-fluoren-1-YL- 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:

: 6344-63-4
1-aminofluorene

: 22251-01-0
N-hydroxyl-1-fluorenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: aq. H₂O₂, maleic anhydride / CH₂Cl₂ / Heating

2: H₂, Et₃N / Pd-C

With maleic anhydride; hydrogen; dihydrogen peroxide; triethylamine; palladium on activated charcoal; In dichloromethane;
DOI:10.1039/j39690000345

Reference yield:

: 7235-17-8
1-Oximino-1,2,3,4-tetrahydro-fluoren

: 22251-01-0
N-hydroxyl-1-fluorenylacetamide

Guidance literature:: Multi-step reaction with 4 steps

1: HCl, AcOH

2: HCl / ethanol / Heating

3: aq. H₂O₂, maleic anhydride / CH₂Cl₂ / Heating

4: H₂, Et₃N / Pd-C

With maleic anhydride; hydrogenchloride; hydrogen; dihydrogen peroxide; acetic acid; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1039/j39690000345

Reference yield:

: 6344-62-3
1-amino-9H-fluoren-9-one

: 22251-01-0
N-hydroxyl-1-fluorenylacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: N₂H₄*H₂O, NaOH, HOCH₂CH₂OH

2: aq. H₂O₂, maleic anhydride / CH₂Cl₂ / Heating

3: H₂, Et₃N / Pd-C

With maleic anhydride; sodium hydroxide; hydrogen; dihydrogen peroxide; hydrazine hydrate; ethylene glycol; triethylamine; palladium on activated charcoal; In dichloromethane;
DOI:10.1039/j39690000345