13706-04-2 Usage
Uses
Used in Organic Synthesis:
2,5-Selenophenedicarboxaldehyde is used as a key intermediate in the synthesis of various organic compounds, contributing to the development of novel materials and pharmaceuticals.
Used in Pharmaceutical Development:
As a member of the selenophene family, 2,5-Selenophenedicarboxaldehyde is utilized in the design and synthesis of new pharmaceutical agents, leveraging its unique chemical properties to enhance drug efficacy and target specific biological pathways.
Used as a Reagent in Chemical Reactions:
2,5-Selenophenedicarboxaldehyde serves as a reagent in the formation of heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Used in Medicinal Chemistry Research:
2,5-Selenophenedicarboxaldehyde is studied for its potential biological activities, such as antioxidant and anti-inflammatory properties, making it an interesting target for further research in the field of medicinal chemistry.
Used in Material Science:
2,5-Selenophenedicarboxaldehyde is employed in the development of new materials with unique properties, such as improved conductivity or stability, by incorporating its selenophene structure into the material's composition.
Check Digit Verification of cas no
The CAS Registry Mumber 13706-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13706-04:
(7*1)+(6*3)+(5*7)+(4*0)+(3*6)+(2*0)+(1*4)=82
82 % 10 = 2
So 13706-04-2 is a valid CAS Registry Number.
13706-04-2Relevant academic research and scientific papers
Heterocyclic compound as well as preparation method and application thereof
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Paragraph 0171; 0178-0180, (2021/08/19)
The invention discloses a heterocyclic compound and a preparation method and application thereof. The invention provides a heterocyclic compound as shown in a formula I or pharmaceutically acceptable salt thereof. The compound has the function of inhibiting the activity of PU.1, and can inhibit the transcriptional activity based on liver cell PU.1 dependence and inhibit fibrosis development.
Five-membered six-membered heterocyclic compound as well as preparation method and application thereof
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Paragraph 0112; 0113; 0114; 0118; 0119; 0120; 0121, (2019/04/26)
The invention relates to a general formula (I) compound and pharmaceutically acceptable salts thereof as well as a preparation method and application thereof. In the general formula (I) compound, X is-aryl-, -heteroaryl-, -heteroaryl-heteroaryl-, and hete
Synthesis, spectroscopy, and reactivity of meso-unsubstituted azuliporphyrins and their heteroanalogues. Oxidative ring contractions to carba-, oxacarba-, thiacarba-, and selenacarbaporphyrins
Lash, Timothy D.,Colby, Denise A.,Graham, Shelley R.,Chaney, Sun T.
, p. 8851 - 8864 (2007/10/03)
This paper reports the first detailed study on meso-unsubstituted azuliporphyrins, an important family of porphyrin-like molecules where one of the usual pyrrole rings has been replaced by an azulene subunit. Although the azulene moiety introduces an elem
