5117-55-5 Usage
General Description
Methyl 3-hydroxy-1-benzofuran-2-carboxylate is a chemical compound with the molecular formula C11H10O4. It is an ester derivative of 3-hydroxy-1-benzofuran-2-carboxylic acid and is commonly used in organic synthesis and medicinal chemistry. Methyl 3-hydroxy-1-benzofuran-2-carboxylate has been found to exhibit various biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties. It is also used as a building block in the synthesis of pharmaceuticals and other organic compounds due to its versatile reactivity and functional group compatibility. Overall, methyl 3-hydroxy-1-benzofuran-2-carboxylate is an important compound with potential applications in the pharmaceutical and chemical industries.
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 articles and documents
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.
