109327-83-5 Usage
Description
1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)is a chemical compound derived from indene, a bicyclic aromatic hydrocarbon. It is characterized by the presence of a hydroxyl group at the 1 position on the indene ring and a 2,3-dihydro substitution, which indicates the addition of two hydrogen atoms across the double bond in the indene ring, resulting in a saturated cyclohexene moiety. The chemical structure and properties of 1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)make it potentially useful in various chemical and pharmaceutical applications, such as in the synthesis of organic compounds or as a building block for drug development.
Uses
Used in Chemical Synthesis:
1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)is used as a building block for the synthesis of various organic compounds. Its unique chemical structure, which includes a hydroxyl group and a saturated cyclohexene moiety, allows for further functionalization and the creation of a wide range of chemical products.
Used in Pharmaceutical Applications:
1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)is used as a starting material for the development of new drugs. Its chemical properties and structural features make it a promising candidate for the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in the Chemical Industry:
1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)is used as an intermediate in the production of various chemical products. Its versatility and reactivity make it a valuable component in the synthesis of a range of industrial chemicals, including dyes, pigments, and specialty chemicals.
Used in Research and Development:
1-(2,3-dihydro-1-hydroxy-1H-inden-1-yl)is used as a research tool in the study of chemical reactions and mechanisms. Its unique structure and properties make it an interesting subject for investigation, potentially leading to new insights and discoveries in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 109327-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,2 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109327-83:
(8*1)+(7*0)+(6*9)+(5*3)+(4*2)+(3*7)+(2*8)+(1*3)=125
125 % 10 = 5
So 109327-83-5 is a valid CAS Registry Number.
109327-83-5Relevant articles and documents
Synthesis of substituted α-tetralones and substituted 1-naphthols via regioselective ring expansion of 1-acyl-1-indanol skeleton
Yang, Te-Fang,Wang, Kuan-Yu,Li, Hsuan-Wei,Tseng, Yang-Chan,Lien, Tai-Chen
, p. 585 - 588 (2012/02/01)
Substituted 1-acyl-1-indanols were prepared using the corresponding readily commercially available substituted indanones as starting materials. Treatment of each 1-acyl-1-indanol derivative with sodium methoxide in hot methanol furnished a regiospecific 2-hydroxy-α-tetralone derivative, which was an α-keto rearrangement product. Each substituted 2-hydroxy-α-tetralone then underwent dehydration to afford the corresponding 1-naphthol derivative.
Electroreductive acylation of aromatic ketones with acylimidazoles
Kise, Naoki,Agui, Syun,Morimoto, Shinji,Ueda, Nasuo
, p. 9407 - 9410 (2007/10/03)
The intermolecular reductive coupling of aromatic ketones with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-trimethylsiloxy ketones and esters. The best result was obtained using Bu4NPF6 as a supporting electrolyte and a Pb cathode in THF. The α-trimethylsiloxy-containing products were transformed to the corresponding α-hydroxy ketones and esters by treatment with TBAF in THF. This method was also effective for the intramolecular reductive coupling of δ- and ε-keto acylimidazoles.
