58621-51-5 Usage
Description
1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is a chemical compound characterized by its molecular formula C12H14O2. It is a ketone derivative featuring a benzofuran ring structure, which contributes to its significance in organic synthesis and medicinal chemistry. 1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is a yellowish liquid at room temperature, soluble in organic solvents, and serves as a crucial building block in the synthesis of pharmaceuticals and agrochemicals. Its potential pharmacological properties, such as anti-inflammatory and antioxidant effects, further enhance its importance in the field of chemistry and pharmaceuticals.
Uses
Used in Pharmaceutical Synthesis:
1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows for the creation of a wide range of therapeutic agents, making it a valuable component in the development of new medications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is used as a key intermediate in the synthesis of various agrochemicals. Its versatility in chemical reactions enables the production of compounds that can be utilized in the development of pesticides, herbicides, and other agricultural products.
Used in Organic Synthesis:
As a ketone derivative with a benzofuran ring, 1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is used as a versatile building block in organic synthesis. Its chemical properties allow for a variety of reactions, making it a valuable component in the creation of complex organic molecules for various applications.
Used in Medicinal Chemistry:
1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is used as a starting material in the development of new drugs due to its potential pharmacological properties. Its anti-inflammatory and antioxidant effects make it a promising candidate for the treatment of various diseases and conditions.
Overall, 1-(2,3-Dihydro-2-methyl-1-benzofuran-5-yl)ethan-1-one is a versatile and important compound with various applications in the fields of chemistry, pharmaceuticals, and agrochemicals, making it a valuable asset in the development of new products and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 58621-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,2 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58621-51:
(7*5)+(6*8)+(5*6)+(4*2)+(3*1)+(2*5)+(1*1)=135
135 % 10 = 5
So 58621-51-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O2/c1-7-5-10-6-9(8(2)12)3-4-11(10)13-7/h3-4,6-7H,5H2,1-2H3
58621-51-5Relevant articles and documents
Activation of phenolic oxygen atom using polyphosphoric acid: Synthesis of carbonyl-containing dihydrobenzofurans/dihydrobenzopyrans
Yang, Qian,Wang, Yu,Yang, Juan,Wu, Yi,Li, Liang-qun,Chen, Fa-ju,Wang, En-hua,Li, Li-lang,Yang, Yan,Yan, Yan-fang,Wang, Li,Ge, Li-juan,Yang, Li-shou,Yang, Xiao-sheng
supporting information, p. 1723 - 1730 (2021/04/09)
Carbonyl-containing dihydrobenzofurans/dihydrobenzopyrans were prepared from carbonyl-containing ortho-allyl/prenylphenols by activation of phenolic oxygen atom using polyphosphoric acid (PPA). Various substrates were investigated, and the corresponding d
Zirconium(IV) chloride catalyzed cyclization of ortho-allylphenols: Synthesis of 2-methyl-2,3-dihydrobenzofurans
Meshram,Premalatha,Rameshbabu,Eeshwaraiah,Yadav
, p. 3091 - 3097 (2007/10/03)
Intramolecular cyclization of ortho-allylphenols has been carried out using zirconium (IV) chloride in mild condition. This method avoids the use of expensive reagents and leads to highly functionalized dihydrobenzofurans.
ACETYLATION, BROMINATION, AND NITRATION OF BENZOXAHETEROCYCLES AND SYNTHESIS OF β-AMINOKETONES FROM ACETYL DERIVATIVES
Daukshas, V. K.,Pyatrauskas, O. Yu.,Udrenaite, E. B.,Gaidyalis, P. G.,Gasperavichene, G. A.
, p. 838 - 841 (2007/10/02)
The method of competing reactions was used to establish the sequence of variation of the relative rates of acetylation, bromination, and nitration reactions of 2-methylcoumaran, chroman, 2,3,4,5-tetrahydrobenzo-1-oxepan, and 1-methoxy-2-ethylbenzene.The i
