160559-13-7 Usage
Description
(2-Hydroxy-phenyl)-propynoic acid ethyl ester is a chemical compound that belongs to the ester class. It is synthesized from ethyl alcohol and propynoic acid, featuring a hydroxyphenyl group. This versatile chemical is known for its unique chemical properties and functional groups, which make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and organic compounds. Additionally, it can be utilized as a flavoring agent in food products, contributing to its potential applications across various fields such as medicine, agriculture, and food science. However, it is crucial to handle and use this compound with care to minimize any potential hazards.
Uses
Used in Pharmaceutical Synthesis:
(2-Hydroxy-phenyl)-propynoic acid ethyl ester is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and medications. Its unique structure allows it to be a building block for various medicinal compounds, enhancing their efficacy and therapeutic potential.
Used in Agrochemical Production:
In the agrochemical industry, (2-Hydroxy-phenyl)-propynoic acid ethyl ester is utilized as a precursor in the production of various agrochemicals. Its functional groups make it suitable for the development of pesticides, herbicides, and other agricultural chemicals that are essential for maintaining crop health and productivity.
Used in Organic Compounds Synthesis:
This ester is also employed in the synthesis of organic compounds, where its hydroxyphenyl group and ester linkage can be manipulated to create a wide range of organic molecules. Its versatility in organic synthesis makes it a valuable asset in the development of new materials and chemical products.
Used as a Flavoring Agent in Food Products:
(2-Hydroxy-phenyl)-propynoic acid ethyl ester finds application as a flavoring agent in the food industry. Its unique chemical properties allow it to impart specific flavors and aromas to food products, enhancing their overall taste and consumer appeal.
Check Digit Verification of cas no
The CAS Registry Mumber 160559-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,5 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 160559-13:
(8*1)+(7*6)+(6*0)+(5*5)+(4*5)+(3*9)+(2*1)+(1*3)=127
127 % 10 = 7
So 160559-13-7 is a valid CAS Registry Number.
160559-13-7Relevant articles and documents
Metal-free annulative hydrosulfonation of propiolate esters: synthesis of 4-sulfonates of coumarins and butenolides
Fernandes, Rodney A.,Gangani, Ashvin J.,Kunkalkar, Rupesh A.
, p. 3970 - 3984 (2020/03/19)
An efficient metal-free and cost-effective method for the synthesis of coumarin and butenolide 4-sulfonates (46 examples) has been developed. The reaction involves addition of sulfonic acids to ethyl propiolates followed by lactonization, resulting in direct formation of coumarin and butenolide 4-sulfonates. This methodology has been elaborated to Sonogashira and Suzuki coupling including the synthesis of rac-tolterodine.
Condensed heteroaromatic ring systems. XXIV. Palladium-catalyzed cyclization of 2-substituted phenylacetylenes in the presence of carbon monoxide
Kondo, Yoshinori,Shiga, Futoshi,Murata, Naoko,Sakamoto, Takao,Yamanaka, Hiroshi
, p. 11803 - 11812 (2007/10/02)
The palladium-catalyzed reaction of 2-alkynylanilines and 2-alkynylphenols in the presence of carbon monoxide and methanol under basic conditions gave the sequential cyclization/carbonylation products, methyl 2-substituted indole and benzo[b]furan-3-carbo
