159448-56-3 Usage
Uses
Used in Pharmaceutical Industry:
2-(5-METHYL-FURAN-2-YL)-BENZOIC ACID METHYL ESTER is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(5-METHYL-FURAN-2-YL)-BENZOIC ACID METHYL ESTER serves as a precursor in the production of agrochemicals, playing a role in the formulation of substances that can protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
2-(5-METHYL-FURAN-2-YL)-BENZOIC ACID METHYL ESTER is utilized as a solvent or reagent in organic synthesis reactions, facilitating the formation of a wide range of chemical products due to its reactive nature.
Used in Fragrance and Flavor Industry:
The aromatic and ester characteristics of 2-(5-METHYL-FURAN-2-YL)-BENZOIC ACID METHYL ESTER make it a valuable component in the fragrance and flavor industry, where it contributes to the creation of various scents and tastes for consumer products.
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 academic research and scientific papers
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.
Imidazole ethers having a II antagonist activity
-
, (2008/06/13)
Compounds of general formula (I) STR1 wherein E is O or S; R is C 1 -C 5 straight, branched or cyclic alkyl or C 2 -C 5 alkenyl; X can be H, F, Cl, Br, I, CF 3 ; n is an integer 1 to 4; m is an integer 0 to 4; A and B are 5- or 6- membered aromatic carboc
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
