1917-16-4 Usage
Description
5-Benzyl-2-furoic acid, a chemical compound with the formula C14H12O3, is a furoic acid derivative featuring a benzyl group attached at the 5-position of the furan ring. This versatile chemical is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. Its unique properties and reactivity make it a valuable building block for synthesizing new molecules with specific functional groups and biological activities, showcasing its promising potential across various fields of science and industry.
Uses
Used in Pharmaceutical Industry:
5-Benzyl-2-furoic acid is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted biological activities, enhancing the effectiveness of treatments in various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 5-benzyl-2-furoic acid is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the development of compounds that can effectively control pests and weeds, thereby contributing to increased crop yields and agricultural productivity.
Used in Organic Synthesis:
5-Benzyl-2-furoic acid serves as a valuable building block in organic synthesis, particularly for the creation of new molecules with specific functional groups. Its reactivity and structural features make it an ideal candidate for the synthesis of complex organic compounds, which can be further utilized in various applications across different industries.
Used in Research and Development:
5-Benzyl-2-furoic acid is employed in research and development settings to explore its potential applications and properties. Scientists and researchers use this compound to investigate its reactivity, stability, and interactions with other molecules, which can lead to the discovery of new chemical reactions and the development of innovative products.
Used in Academic Education:
In academic settings, 5-benzyl-2-furoic acid is utilized as a teaching aid to help students understand the principles of organic chemistry, medicinal chemistry, and related fields. Its unique structure and properties provide a practical example for students to learn about the synthesis, reactions, and applications of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1917-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1917-16:
(6*1)+(5*9)+(4*1)+(3*7)+(2*1)+(1*6)=84
84 % 10 = 4
So 1917-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O3/c13-12(14)11-7-6-10(15-11)8-9-4-2-1-3-5-9/h1-7H,8H2,(H,13,14)
1917-16-4Relevant articles and documents
Regioselective and Stereoselective Pd-Catalyzed Intramolecular Arylation of Furans: Access to Spirooxindoles and 5H-Furo[2,3-c]quinolin-4-ones
Liu, Jianchao,Peng, Hui,Yang, Yongjie,Jiang, Huanfeng,Yin, Biaolin
, p. 9695 - 9706 (2016/11/02)
Herein, we report regio- and stereoselective intramolecular direct arylations of N-(2-bromophenyl)-2-furancarboxamides 1 to produce spirooxindoles 2 and 5H-furo[2,3-c]quinolin-4-ones 3 under different reaction conditions. Specifically, in the presence of
NOVEL PROCESSES FOR THE PREPARATION OF SUBSTITUTED PROPENONE DERIVATIVES
-
Page 3, (2010/11/30)
The present invention provides industrial and commercial processes for the preparation of 2-acyl-5-benzylfuran derivatives, 1,2,4-triazole-3-carboxylic acid ester derivatives and propenone derivatives having anti-HIV activities and usuful crystals thereof. wherein R1, R2 and R4 each is independently hydrogen or the like; A is CR6 or N; R6 is hydrogen or the like; Q is a protecting group; and L is a leaving group.
