| Identification | More | [Name]
N-Phenylbenzohydroxamic acid | [CAS]
304-88-1 | [Synonyms]
N-BENZOYL-N-PHENYLHYDROXYLAMINE
N-BENZOYLPHENYLHYDROXYLAMINE
N-HYDROXY-N-PHENYLBENZAMIDE
N-PHENYLBENZOHYDROXAMIC ACID
TANTALON
Benzamide, N-hydroxy-N-phenyl-
Benzohydroxamic acid, N-phenyl-
BPHA
N-Benzoyl-N-phenylhydroxamic acid
N-Benzoyl-N-phenylhydroxylamin
N-Hydroxybenzanilide
n-hydroxy-n-phenyl-benzamid
N-Phenylbenzohyroxamic acid
N-BENZOYL-N-PHENYL-HYDROXYLAMINE*CRYSTALLINE
N-Hydroxy-N-phenylbenzamide, N-Phenylbenzohydroxamic acid | [EINECS(EC#)]
206-158-9 | [Molecular Formula]
C13H11NO2 | [MDL Number]
MFCD00002111 | [Molecular Weight]
213.23 | [MOL File]
304-88-1.mol |
| Chemical Properties | Back Directory | [Appearance]
off-white fibrous powder | [Melting point ]
118-120 °C(lit.) | [Boiling point ]
353.22°C (rough estimate) | [density ]
1.1544 (rough estimate) | [refractive index ]
1.5700 (estimate) | [storage temp. ]
2-8°C
| [Water Solubility ]
Practically insoluble in water | [form ]
Needle-Like Crystals or Crystalline Powder | [pka]
8.09±0.19(Predicted) | [color ]
Light beige needle-like | [Stability:]
Stable. Incompatible with strong oxidizing agents. | [BRN ]
2212449 | [InChI]
InChI=1S/C13H11NO2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,16H | [InChIKey]
YLYIXDZITBMCIW-UHFFFAOYSA-N | [SMILES]
C(N(O)C1=CC=CC=C1)(=O)C1=CC=CC=C1 | [CAS DataBase Reference]
304-88-1(CAS DataBase Reference) | [NIST Chemistry Reference]
N-benzoyl-n-phenylhydroxylamine(304-88-1) | [EPA Substance Registry System]
304-88-1(EPA Substance) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29280000 |
| Hazard Information | Back Directory | [Chemical Properties]
off-white fibrous powder | [Uses]
N-Benzoyl-N-phenylhydroxylamine was used as a complexing agent for studying the dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO) behavior of vanadium (V). It was used as an extractant in the determination of beryllium in natural waters. | [General Description]
The mechanism of the reaction of N-benzoyl-N-phenylhydroxylamine with vanadium(IV) was studied. | [Synthesis]
The general procedure for the synthesis of N-benzoylphenylhydroxylamine from benzaldehyde and nitrobenzene: the reaction was carried out under the catalytic conditions of different imidazolium and triazolium salts, and it was found that triazolium salts with lower spatial site resistance significantly increased the yield of the product, N-benzoylphenylhydroxylamine (see Table 1). The experimental results showed that the reaction could be carried out efficiently even at catalyst concentrations as low as 0.125 mol%. Table 1 details the reaction conditions for the preparation of N-benzoylphenylhydroxylamine. | [Purification Methods]
Recrystallise it from hot water, *benzene Et2O/hexane or acetic acid. It complexes with metals. [Beilstein 15 III 8, 15 IV 7.] | [References]
[1] Advanced Synthesis and Catalysis, 2011, vol. 353, # 4, p. 624 - 629
[2] Patent: WO2008/115153, 2008, A1. Location in patent: Page/Page column 27-28
[3] Patent: WO2008/115153, 2008, A1. Location in patent: Page/Page column 41-42
[4] Patent: WO2008/115153, 2008, A1. Location in patent: Page/Page column 41-42
[5] Patent: WO2008/115153, 2008, A1. Location in patent: Page/Page column 41-42 |
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