15909-81-6 Usage
Description
(diethylcarbamimidoyl)selanyl, also known as DECSe, is a chemical compound belonging to the organoselenium compound family. It features a carbamimidoyl group attached to a selenium atom, which contributes to its unique properties and potential applications in various fields.
Uses
Used in Organic Chemistry:
DECSe is utilized as a reagent in organic chemistry for the synthesis of various organic compounds, taking advantage of its unique chemical structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, DECSe has been studied for its antioxidant and anti-inflammatory properties, making it a promising candidate for drug discovery and development.
Used in Synthesis of Selenium-Containing Materials:
DECSe has been investigated as a potential precursor in the synthesis of selenium-containing materials, which could have applications in various industries, including pharmaceuticals and materials science.
Used as a Catalyst:
Additionally, DECSe has been explored for its potential as a catalyst in various chemical reactions, further expanding its utility in the chemical sciences.
Safety Precaution:
It is crucial to handle DECSe with care, as selenium compounds can be toxic and potentially hazardous to health. Proper safety measures should be taken during its use and storage to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 15909-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,0 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15909-81:
(7*1)+(6*5)+(5*9)+(4*0)+(3*9)+(2*8)+(1*1)=126
126 % 10 = 6
So 15909-81-6 is a valid CAS Registry Number.
15909-81-6Relevant articles and documents
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Zingaro et al.
, p. 292,294 (1953)
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Selenocarbonyl synthesis using Woollins reagent
Bhattacharyya, Pravat,Woollins
, p. 5949 - 5951 (2007/10/03)
[PhP(Se)(μ-Se)]2 selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130°C in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25°C.
