331714-58-0 Usage
Uses
Used in Organic Synthesis:
1,3-Benzenedicarbonitrile, 5-formyl(9CI) is used as a building block for the synthesis of various organic compounds and dyes. Its unique structure allows for the creation of a wide range of products with diverse applications across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3-Benzenedicarbonitrile, 5-formyl(9CI) is used as a starting material for the development of new drugs. Its potential applications in this field are attributed to its ability to be incorporated into complex molecular structures that can target specific biological pathways.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1,3-Benzenedicarbonitrile, 5-formyl(9CI) is employed for the development of new pesticides. Its role in this sector is due to its potential to be part of molecules that can effectively control, repel, or kill pests while minimizing environmental impact.
It is crucial to handle 1,3-Benzenedicarbonitrile, 5-formyl(9CI) with care, as it may pose risks to human health and the environment. Proper safety measures and disposal methods should be adhered to when working with 1,3-Benzenedicarbonitrile, 5-formyl- (9CI).
Check Digit Verification of cas no
The CAS Registry Mumber 331714-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,7,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 331714-58:
(8*3)+(7*3)+(6*1)+(5*7)+(4*1)+(3*4)+(2*5)+(1*8)=120
120 % 10 = 0
So 331714-58-0 is a valid CAS Registry Number.
331714-58-0Relevant articles and documents
PYRIDONE DERIVATIVES AS NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS
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Page/Page column 39, (2010/04/03)
The present invention relates to 2-pyridone derivatives of Formula (I) or (IV) as herein described, compositions containing such compounds, synthetic processes for making such compounds, and therapeutic methods that include the administration of such comp
Synthesis, absorption and luminescence of a new series of soluble distyrylbenzenes featuring cyano substituents at the peripheral rings
Schweikart, Karl-Heinz,Hanack, Michael,Lueer, Larry,Oelkrug, Dieter
, p. 293 - 302 (2007/10/03)
The synthesis of a complete series of nine soluble distyrylbenzenes (DSBs) with two (2a-c) and four cyano groups (1a-f) attached to the peripheral aromatic rings is reported. They were prepared by the Wittig reaction and characterized by 1H and 13C NMR, FT-IR, UV/Vis, PL, EL, mass spectra, and elemental analysis. The optical properties have been studied in detail to monitor structure-luminescence relationships as a function of the position of the cyano moieties. The DSBs with cyano substituents show bathochromic shifts in their absorption spectra when compared to the parent DSB (30). The extent of this red-shift depends on electronic and steric factors. The bis(p-cyano)-substituted compound 2c exhibits a small Stokes shift and a remarkably high quantum yield of ψF = 0.6-0.8 in the solid state. All the new distyrylbenzenes show electroluminescence when employed in devices with an ITO/PcCu/DSB/Al configuration and with colors ranging from red to green.
