111080-50-3 Usage
Description
2-Ethyl-2,3-dihydrobenzofuran-2-carboxylic acid, also known as EDBC, is a chemical compound characterized by its distinctive molecular structure that features a benzofuran ring and a carboxylic acid group. It is a white powder that is soluble in organic solvents, with a molecular weight of 236.26 g/mol. EDBC's unique chemical properties make it a promising candidate for various applications, particularly in the pharmaceutical industry, due to its potential as an anti-inflammatory and anti-tumor agent, as well as its utility in the synthesis of organic compounds.
Uses
Used in Pharmaceutical Industry:
2-Ethyl-2,3-dihydrobenzofuran-2-carboxylic acid is used as a pharmaceutical intermediate for its potential anti-inflammatory and anti-tumor properties. Its unique molecular structure allows it to be a valuable building block in the creation of pharmaceuticals and other biologically active molecules.
Used in Organic Synthesis:
EDBC is used as a key component in the synthesis of various organic compounds, leveraging its chemical reactivity and solubility in organic solvents to facilitate the production of complex molecules.
Used in Research and Development:
2-Ethyl-2,3-dihydrobenzofuran-2-carboxylic acid is utilized in research settings to explore its potential applications and effects further. Ongoing studies aim to understand its full capabilities and optimize its use in various fields, including medicine and chemistry.
While the specific applications of EDBC in different industries are not explicitly detailed in the provided materials, its potential uses in the pharmaceutical industry, organic synthesis, and research and development are inferred from its described properties and potential. Further research is necessary to fully realize its applications and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 111080-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,8 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 111080-50:
(8*1)+(7*1)+(6*1)+(5*0)+(4*8)+(3*0)+(2*5)+(1*0)=63
63 % 10 = 3
So 111080-50-3 is a valid CAS Registry Number.
111080-50-3Relevant articles and documents
A new efficient synthesis of efaroxan
Mayer,Brunel,Imbert
, p. 3021 - 3022 (2007/10/03)
The key step of the synthesis of efaroxan was the dihydrobenzofuran ring formation involving an intramolecular cyclization of the tertiary alcohol intermediate with the fluoroaromatic moiety in basic medium. This carbinol was prepared according to two rou
A new approach to the synthesis of efaroxan
Couture,Gouverneur,Mioskowski
, p. 3023 - 3026 (2007/10/03)
Efaroxan was synthetised by cyclisation of the tertiary alcohol 2 which was prepared by the ring opening of the gem-disubstituted epoxide 3 with ortho-metallated fluorobenzene.
α-Adrenoreceptor Reagents. 2. Effects of Modification of the 1,4-Benzodioxan Ring System on α-Adrenoreceptor Activity
Chapleo, Christopher B.,Myers, Peter L.,Butler, Richard C. M.,Davis, John A.,Doxey, John C.,et al.
, p. 570 - 576 (2007/10/02)
Modification of the 1,4-benzodioxan ring present in RX 781094 (1) has not previously been considered.This paper describes a number of analogues of this ring system, including compounds in which one of the oxygen atoms has been replaced by a methylene group and also those in which the ring size has been changed to give, for example, furan and thiophene derivatives.The dihydroxybenzofuranylimidazoline compound 7 is the only analogue possesing presynaptic antagonist potency and selectivity comparable to that of 1.In view of this result, a number of derivatives was prepared to determine the structure-activity relationships within this series.Many derivatives, as well as the parent compound 7, were found to possess presynaptic α2-adrenoreceptor antagonist and postsynaptic α1-adrenoreceptor partial agonist properties.Two of the selective presynaptic antagonists,13 and 14, possess greater potency and selectivity than that possessed by 1.The 5-chloro derivative 25 is twice as potent as 1 after oral administration but only about half as potent when given intravenously.
