159448-56-3 Usage
General Description
The chemical compound 2-(5-Methyl-furan-2-yl)-benzoic acid methyl ester is a methyl ester of benzoic acid with a furan ring substitution. It is a synthetic organic compound commonly used in the production of pharmaceuticals, agrochemicals, and other industrial applications. As a methyl ester, it is often used as a solvent or as a reagent in organic synthesis reactions. Its chemical properties make it a valuable building block for creating a wide range of bioactive compounds and functional materials. Additionally, its aromatic and ester functionalities also make it useful in the fragrance and flavor industry.
Check Digit Verification of cas no
The CAS Registry Mumber 159448-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,4 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159448-56:
(8*1)+(7*5)+(6*9)+(5*4)+(4*4)+(3*8)+(2*5)+(1*6)=173
173 % 10 = 3
So 159448-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O3/c1-9-7-8-12(16-9)10-5-3-4-6-11(10)13(14)15-2/h3-8H,1-2H3
159448-56-3Relevant articles and documents
AgONO-Assisted Direct C-H Arylation of Heteroarenes with Anilines
Gowrisankar, Saravanan,Seayad, Jayasree
supporting information, p. 12754 - 12758 (2015/03/30)
A novel copper-catalyzed C-H arylation of heteroarenes with anilines by an in situ diazonium reaction is established by using silver nitrite (AgONO) as an unconventional nitrosating reagent under acid-free conditions. It provides a complementary approach for the C-H arylation of electron-rich heteroarenes with aromatic amines affording a variety of heterobiaryls in moderate to good yields.
Nonpeptide Angiotensin II Receptor Antagonists. Synthesis, in Vitro Activity, and Molecular Modeling Studies of N-imidazoles
Salimbeni, Aldo,Canevotti, Renato,Paleari, Fabio,Bonaccorsi, Fabrizio,Renzetti, Anna R.,et al.
, p. 3928 - 3938 (2007/10/02)
With the aim of explaining the influence of the structural changes on the biphenylic moiety on the activity, a series of N-imidazoles (I), constructed on the model of DuPont compounds by replacing either the central or terminal pheny
