BENZENESELENINIC ACID
BENZENESELENINIC ACID Basic information
- Product Name:
- BENZENESELENINIC ACID
- Synonyms:
-
- benzene selenoic acid
- seleninobenzoic acid
- BENZENESELENINIC ACID 99%
- PHENYLSELENIOUSACID
- Benzene Selenenic Acid
- BENZENESELENIC ACID
- BENZENESELENINIC ACID
- PHENYLSELENIC ACID
- CAS:
- 6996-92-5
- MF:
- C6H6O2Se
- MW:
- 189.07
- EINECS:
- 230-271-2
- Product Categories:
-
- Pharmaceutical Intermediates
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Classes of Metal Compounds
- Oxidation
- Se (Selenium) Compounds
- Semimetal Compounds
- Synthetic Organic Chemistry
- Building Blocks
- Organic Building Blocks
- Selenium Compounds
- Mol File:
- 6996-92-5.mol
BENZENESELENINIC ACID Chemical Properties
- Melting point:
- 121-124 °C (lit.)
- Boiling point:
- 114.4±23.0 °C(Predicted)
- Density
- 1.9300
- Water Solubility
- Slightly soluble in water
- pka
- pK1:4.79 (25°C)
- form
- solid
- color
- Plates from water
- BRN
- 1929765
- CAS DataBase Reference
- 6996-92-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- T,N
- Risk Statements
- 23/25-33-50/53
- Safety Statements
- 20/21-28-45-60-61
- RIDADR
- UN 3283 6.1/PG 2
- WGK Germany
- 3
- F
- 8
- HazardClass
- 6.1(b)
- PackingGroup
- III
- HS Code
- 29310099
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
BENZENESELENINIC ACID Usage And Synthesis
Chemical Properties
white to beige crystalline powder or needles
Uses
Benzeneseleninic acid was used as catalyst during the oxidation of sulfides to sulfoxides via ligand coupling on the iodine atom. It was also used in the preparation of 3-methoxy-17a-oxa-D-homoestra-l,3,5(10)-trien-17-one.
General Description
Benzeneseleninic acid oxidizes hydrazine or 1,2-disubstituted derivatives to corresponding diazenes.
Safety Profile
Reacts violently with hydrazinederivatives (e.g., benzohydrazide). When heated todecomposition it emits toxic fumes of Se.
Purification Methods
Add 10% excess of 15M NH3 to the solid acid and stir until the solid dissolves, filter, decolorise with charcoal (2x, Norite) and acidify by slow addition of 6M HCl, filter the solid off and wash it with H2O. Dissolve the acid in the minimum volume of MeOH, and this solution is added dropwise to boiling H2O until cloudiness appears. At this point add 25% more boiling H2O, filter hot (decolorise if necessary) and cool rapidly, with scratching, to 0o. After 30minutes the solid is filtered off and recrystallised as before but with very slow cooling. The colourless needles are filtered off and dried in a vacuum desiccator (CaCl2) before the melting point is measured [McCullough & Gould J Am Chem Soc 71 674 1949]. The HNO3 complex has m 112o. [Beilstein 11 H 422, 11 I 110, 11 III 716.]
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