P29006
Phenylphosphonic acid
98%
Sinonimo/i:
Benzene phosphonic acid
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5 G
CHF 57.80
100 G
CHF 77.00
500 G
CHF 256.00
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Cambia visualizzazione
5 G
CHF 57.80
100 G
CHF 77.00
500 G
CHF 256.00
About This Item
Formula condensata:
C6H5P(O)(OH)2
Numero CAS:
Peso molecolare:
158.09
Beilstein:
2245168
Numero CE:
Numero MDL:
Codice UNSPSC:
12352300
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
Livello qualitativo
Saggio
98%
Stato
crystals
Punto di fusione
162-164 °C (lit.)
Stringa SMILE
OP(O)(=O)c1ccccc1
InChI
1S/C6H7O3P/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H2,7,8,9)
QLZHNIAADXEJJP-UHFFFAOYSA-N
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Applicazioni
Additive used with Noyori's catalyst for oxidation of sulfides to sulfones.
Noyori Oxidation (Sodium Tungstate Dihydrate, Hydrogen Peroxide, Methyltri-n-octylammonium Hydrogen Sulfate, Phosphonic Acid)
Noyori Oxidation (Sodium Tungstate Dihydrate, Hydrogen Peroxide, Methyltri-n-octylammonium Hydrogen Sulfate, Phosphonic Acid)
Self assembled monolayers (SAMs)of phenylphosphonic acid may be used to make the interface between organic semiconductors and transparent conductive oxides.[1] The acid may be used to functionalize titania particles.[2] Additive used with Noyorι¢s catalyst for greener oxidation of sulfides to sulfones.
Avvertenze
Danger
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 4 Oral - Skin Corr. 1B
Codice della classe di stoccaggio
8A - Combustible corrosive hazardous materials
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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I clienti hanno visto anche
Important reaction parameters in the synthesis of phenylphosphonic acid functionalized titania particles by reactive milling.
Betke A and Kickelbick G
New. J. Chem., 38(3), 1264-1270 (2014)
T Q Duong et al.
Magnetic resonance in medicine, 45(5), 801-810 (2001-04-27)
The apparent diffusion coefficients (ADCs) of a series of markers concentrated in the extracellular space of normal rat brain were measured to evaluate, by inference, the ADC of water in the extracellular space. The markers (mannitol, phenylphosphonate, and polyethylene glycols)
Justin L Ford et al.
Helicobacter, 12(6), 609-615 (2007-11-16)
Helicobacter pylori can utilize phenylphosphonate as a sole source of phosphorus, and it is able to transport the phosphonate N-phosphonoacetyl-L-aspartate. However, H. pylori does not have any genes homologous to those of the known pathways for phosphonate degradation in bacteria
Zhaohui Cui et al.
Langmuir : the ACS journal of surfaces and colloids, 26(1), 179-182 (2009-08-04)
The in situ crystallization technique has been utilized to fabricate zirconium phenylphosphonate (ZrPP) films with their hexagonal crystallite perpendicular to the copper substrate. The micro/nano roughness surface structure, as well as the intrinsic hydrophobic characteristic of the surface functional groups
Christel Gervais et al.
Magnetic resonance in chemistry : MRC, 42(5), 445-452 (2004-04-20)
1H, 13C, 17O and 31P NMR parameters, including chemical shift tensors and quadrupolar parameters for 17O, were calculated for phenylphosphonic acid, C6H5PO(OH)2, under periodic boundary conditions. The results are in very good agreement with experimental data and permit the unambiguous
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