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BENZENESELENINIC ACID

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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
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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)
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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
8
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29310099

MSDS

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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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