317385-62-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-Thiophenecarboxylic acid N-butyl ester is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure allows it to be a key component in the development of new drugs and agricultural products, contributing to advancements in these fields.
Used as a Solvent:
3-THIOPHENECARBOXYLIC ACID N-BUTYL ESTER is also employed as a solvent in various chemical processes. Its properties make it suitable for dissolving a range of substances, facilitating reactions and improving the efficiency of industrial processes.
Used in Fragrance and Flavoring Industries:
3-Thiophenecarboxylic acid N-butyl ester is used in the manufacture of fragrances and flavorings, where its unique chemical characteristics contribute to the creation of distinct scents and tastes in consumer products.
Used in Organic Synthesis:
3-THIOPHENECARBOXYLIC ACID N-BUTYL ESTER has potential applications in organic synthesis, where it can be used as a building block for the production of other organic compounds. Its versatility in chemical reactions makes it a valuable asset in the synthesis of complex organic molecules.
Used in Research:
3-Thiophenecarboxylic acid N-butyl ester is also valuable in research settings, where its unique properties can be explored for new applications and to enhance understanding of chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 317385-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,8 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 317385-62:
(8*3)+(7*1)+(6*7)+(5*3)+(4*8)+(3*5)+(2*6)+(1*2)=149
149 % 10 = 9
So 317385-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2S/c1-2-3-5-11-9(10)8-4-6-12-7-8/h4,6-7H,2-3,5H2,1H3
317385-62-9Relevant academic research and scientific papers
Efficient carbonylation of aryl and heteroaryl bromides under atmospheric pressure of CO
Yang, Weizhun,Han, Wei,Zhang, Weidong,Shan, Lei,Sun, Jiansong
supporting information; experimental part, p. 2253 - 2255 (2011/10/19)
In the presence of Et and n-BuOH, efficient alkoxycarbonylation of (hetero)aromatic bromides was achieved under atmospheric pressure of carbon monoxide with in situ generated palladium/rac-BINAP as catalyst. Georg Thieme Verlag Stuttgart - New York.
Efficient carbonylation of aryl and heteroaryl bromides using a palladium/diadamantylbutylphosphine catalyst
Neumann, Helfried,Brennfuehrer, Anne,Gross, Peter,Riermeier, Thomas,Almena, Juan,Beller, Matthias
, p. 1255 - 1261 (2007/10/03)
A general palladium-catalyzed alkoxycarbonylation of aryl and heteroaryl bromides has been developed in the presence of bulky monodentate phosphines. Studies of the butoxycarbonylation of three model substrates revealed the advantages of di-1-adamantyl-n-butylphosphine compared to other ligands. In the presence of this catalyst system various bromoarenes provided the corresponding benzoic acid derivatives (ester, amides, acids) in excellent yield at low catalyst loadings (0.5 mol% Pd or below).
