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262-05-5

  • Product Name:10H-phenoselenazine
  • Molecular Formula:C10H9NSe
  • Molecular Weight:246.17
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Product Details

Purity:99%

99% Purity Commercial production 10H-phenoselenazine 262-05-5 with Cheapest Price

  • Molecular Formula:C10H9NSe
  • Molecular Weight:246.17
  • Vapor Pressure:1.23E-05mmHg at 25°C 
  • Boiling Point:307.5 °C at 760 mmHg 
  • Flash Point:139.8 °C 
  • PSA:12.03000 
  • LogP:1.53660 

10H-Phenoselenazine(Cas 262-05-5) Usage

Chemical Composition and Structure

10H-Phenoselenazine is a chemical compound which consists of carbon, hydrogen, nitrogen, and selenium atoms. The compound exhibits specific chemical properties, including a melting point of 194-196°C (measured in benzene or hexane) and a predicted boiling point of 424.1±37.0°C.

Production Methods

10H-Phenoselenazine can be synthesized through a chemical reaction using (2-nitrobenzene)phenylselenyl ether as the raw material under nitrogen conditions in the presence of a reducing agent such as triphenylphosphine.

General Description

10H-Phenoselenazine is a chemical compound with the molecular formula C13H9NSe. It is a heterocyclic compound containing a selenazole ring, and it is also known as benzoselenadiazole. 10H-Phenoselenazine is a potential candidate for pharmaceutical research due to its diverse biological activities, including anti-cancer, anti-bacterial, and anti-inflammatory properties. The compound has shown promising results in inhibiting the growth of cancer cells and reducing inflammation in experimental studies. Its unique structure and potential pharmacological properties make 10H-Phenoselenazine an interesting target for further research and development in the field of medicinal chemistry.

InChI:InChI=1/C12H9NSe/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H

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The TeII/TeIII-catalyzed dehydrogenative...

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262-05-5 Process route

2-(phenylseleno)nitrobenzene
65848-40-0

2-(phenylseleno)nitrobenzene

phenoselenazine
262-05-5

phenoselenazine

Conditions
Conditions Yield
With triphenylphosphine; In 1,2-dichloro-benzene; at 180 ℃; for 30h; Reagent/catalyst; Solvent; Concentration; Inert atmosphere;
92%
With triphenylphosphine; In 1,2-dichloro-benzene; at 180 ℃; for 24h; Inert atmosphere; Sealed tube; Schlenk technique;
68%
With triphenylphosphine; In 1,2-dichloro-benzene; at 180 ℃; for 24h; Inert atmosphere;
54%
diphenylamine
122-39-4

diphenylamine

phenoselenazine
262-05-5

phenoselenazine

Conditions
Conditions Yield
With sulenium monochloride; In toluene; for 5h; Heating / reflux;
20%
With selenium(IV) oxide; selenium; iodine; In sulfolane; at 150 ℃; for 5h; Sealed tube;
20%
With selenium(IV) oxide; selenium; iodine; In sulfolane; at 150 ℃;
16%
With selenium tetrachloride; benzene;
With chloroform; diselenium dichloride;
With selenium(IV) oxide; selenium; iodine; In sulfolane;

262-05-5 Upstream products

  • 122-39-4
    122-39-4

    diphenylamine

  • 65848-40-0
    65848-40-0

    2-(phenylseleno)nitrobenzene

  • 552-16-9
    552-16-9

    ortho-nitrobenzoic acid

  • 1666-13-3
    1666-13-3

    diphenyl diselenide

262-05-5 Downstream products

  • 86-74-8
    86-74-8

    9H-carbazole

  • 2934-35-2
    2934-35-2

    10-<3-Dimethylamino-propyl>-2-propionyl-phenselenazin

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