39178-60-4 Usage
Uses
Used in Research and Industrial Synthesis:
5-Bromo-2-ethylbenzofuran is used as a reagent or intermediate for the synthesis of more complex chemical compounds. Its unique structure and properties make it a valuable component in the development of new chemical entities.
Used in Chemical Research:
5-Bromo-2-ethylbenzofuran is used as a research compound to explore its chemical properties, reactivity, and potential applications in various chemical reactions. It can provide insights into the benzofuran family of compounds and contribute to the advancement of organic chemistry.
Used in Pharmaceutical Development:
Although its biological effects are largely unknown, 5-Bromo-2-ethylbenzofuran may be used in pharmaceutical research to investigate its potential as a precursor for the development of new drugs or drug candidates. Its unique structure could offer novel therapeutic opportunities.
Used in Material Science:
5-Bromo-2-ethylbenzofuran may have potential applications in material science, particularly in the development of new materials with specific properties. Its unique structure and chemical properties could contribute to the creation of innovative materials for various industries.
Used in Environmental Applications:
While not well-studied, 5-Bromo-2-ethylbenzofuran could potentially be used in environmental applications, such as the development of new methods for pollution control or the synthesis of environmentally friendly materials. Further research would be required to explore these possibilities.
Check Digit Verification of cas no
The CAS Registry Mumber 39178-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39178-60:
(7*3)+(6*9)+(5*1)+(4*7)+(3*8)+(2*6)+(1*0)=144
144 % 10 = 4
So 39178-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9BrO/c1-2-9-6-7-5-8(11)3-4-10(7)12-9/h3-6H,2H2,1H3
39178-60-4Relevant academic research and scientific papers
Synthesis and reduction of 5-halo-and 5-nitro-1-(benzofuran-3-yl)-2- phenylethanones
Kwiecien,Szychowska
, p. 1002 - 1009 (2008/09/16)
Novel 1-(2-alkylbenzofuran-3-yl)-2-(4-methoxyphenyl)ethanones having a halogen or nitro group in position 5 of the benzofuran ring were synthesized starting with the corresponding 2-(2-formylphenoxy)alkanoic acids. 1-(2-Alkylbenzofuran-3-yl)-2-phenylethanols containing bromine or chlorine atom were prepared in high yields by reduction of the corresponding ethanones with lithium aluminum hydride. Selective catalytic reduction of nitro 1-(2-alkylbenzofuran-3-yl)-2-(4-methoxyphenyl)ethanones to the corresponding amino compounds under Pd/C in room temperature was achieved.
Sulfonamide compounds and medicinal use thereof
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Page column 70, (2010/02/04)
A sulfonamide compound of the formula (I):R 1 --SO 2 NHCO--A--R 2 (I)wherein R 1 is alkyl, alkenyl, alkynyl and the like; A is an optionally substituted heteropolycyclic group except benzimidazolyl, indolyl, 4,7-dihydrobenzimidazolyl and 2,3-dihydrobenzoxazinyl; X is alkylene, oxa, oxa(lower)alkylene and the like; and R 2 is optionally substituted aryl, substituted biphenylyl and the like, a salt thereof and a pharmaceutical composition comprising the same. The sulfonamide compound is effective for the diseases treatable based on their blood sugar level-depressing activity, cGMP-PDE (especially PDE-V)-inhibiting activity, smooth muscle relaxing activity, bronchodilating activity, vasodilating activity, smooth muscle cell suppressing activity, and antiallergic activity.
