425645-31-4 Usage
Uses
Used in Pharmaceutical Synthesis:
5-(4-METHYL-2-NITROPHENYL)-2-FURALDEHYDE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex organic molecules.
Used in Organic Material Synthesis:
In the field of organic materials, 5-(4-METHYL-2-NITROPHENYL)-2-FURALDEHYDE is used as a building block for creating various organic compounds, taking advantage of its furan and nitrophenyl groups.
Safety Considerations:
It is important to handle 5-(4-METHYL-2-NITROPHENYL)-2-FURALDEHYDE with care, as it may be harmful if ingested or inhaled, and it can cause skin and eye irritation. Proper safety measures should be taken during its use in laboratories and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 425645-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,5,6,4 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 425645-31:
(8*4)+(7*2)+(6*5)+(5*6)+(4*4)+(3*5)+(2*3)+(1*1)=144
144 % 10 = 4
So 425645-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO4/c1-8-2-4-10(11(6-8)13(15)16)12-5-3-9(7-14)17-12/h2-7H,1H3
425645-31-4Relevant academic research and scientific papers
A new simple route to the thieno[2,3-b]indole ring system
Butin, Alexander V.,Tsiunchik, Fatima A.,Abaev, Vladimir T.,Zavodnik, Valery E.
experimental part, p. 1145 - 1148 (2009/04/06)
A simple and effective method has been elaborated for the synthesis of thieno[2,3-b]indole ring system. It is based on the electrophilic recyclization of 2-alkyl-5-(2-isothiocyanoaryl)furans in the presence of anhydrous AlCl 3. Georg Thieme Ver
Furan as a 1,3-diketone equivalent: the second type furan recyclization applied to indole synthesis
Butin, Alexander V.
, p. 4113 - 4116 (2007/10/03)
A new approach for the synthesis of indole derivatives based on protolytic recyclization of 2-alkyl-5-(2-tosylaminoaryl)-furans is described. The furan ring in this unusual transformation formally serves as a 1,3-diketone equivalent.
