5117-55-5 Usage
Uses
Used in Organic Synthesis:
Methyl 3-hydroxy-1-benzofuran-2-carboxylate is used as a building block in organic synthesis for its ability to contribute to the formation of a wide range of organic compounds. Its functional groups make it a valuable intermediate in the creation of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methyl 3-hydroxy-1-benzofuran-2-carboxylate is used as a key component in the synthesis of pharmaceuticals. Its biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties, make it a promising candidate for the development of new drugs.
Used in Pharmaceutical Industry:
Methyl 3-hydroxy-1-benzofuran-2-carboxylate is utilized in the pharmaceutical industry as a precursor for the production of various drugs. Its versatility and reactivity allow for the creation of compounds with potential therapeutic applications.
Used in Chemical Industry:
The chemical industry employs Methyl 3-hydroxy-1-benzofuran-2-carboxylate for its potential in creating new chemical entities and improving existing chemical processes. Its compatibility with different functional groups makes it a valuable asset in the synthesis of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 5117-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5117-55:
(6*5)+(5*1)+(4*1)+(3*7)+(2*5)+(1*5)=75
75 % 10 = 5
So 5117-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O4/c1-13-10(12)9-8(11)6-4-2-3-5-7(6)14-9/h2-5,12H,1H3/b10-9-
5117-55-5Relevant academic research and scientific papers
APPLICATION OF MAGNESIUM ALKOXIDES TO SYNTHESES OF BENZOHETEROCYCLIC COMPOUNDS
Svoboda, Jiri,Nic, Miloslav,Palecek, Jaroslav
, p. 592 - 599 (2007/10/02)
The Dieckmann condensations of methyl -X-acetates Ia-Ih (X = O, S, SO2, NH, NCH3) initiated by action of magnesium methoxide, ethoxide, isopropoxide and other basic reagents have been studied under various conditions.Whereas magnesium methoxide has comparable efficiency as sodium methoxide and potassium tert-butoxide in syntheses of benzoheterocyclic compounds IIa-IIh, magnesium ethoxide gives the ethyl ester IIb in a medium yield, and magnesium isopropoxide is quite inefficient in the condensation reaction.The alkylation of the esters IIa, IId, and IIg with methyl chloroaetate in the presence of sodium hydride in dimethylformamide gives the diesters IIi-IIk which on action by potassium tert-butoxide undergo the cyclization reaction to give esters III.
