40513-50-6 Usage
Physical appearance
White crystalline solid 2,3-Dihydro-7-hydroxy-3-methyl-1H-inden-1-one appears as a white solid with a crystalline structure.
Solubility
Soluble in organic solvents It can dissolve in organic solvents, which is a common property of many chemical compounds.
Uses
Production of pharmaceuticals and agrochemicals 2,3-Dihydro-7-hydroxy-3-methyl-1H-inden-1-one is used as a starting material or intermediate in the synthesis of various pharmaceuticals and agrochemicals.
Potential applications
Organic synthesis It may be used as a building block or reagent in the synthesis of other organic compounds, opening up new possibilities in the field of organic chemistry.
Antioxidant properties
Ability to neutralize free radicals The compound has been found to possess antioxidant properties, which means it can help neutralize free radicals and potentially prevent oxidative damage in various systems.
Anti-inflammatory properties
Reduction of inflammation It also exhibits anti-inflammatory properties, which could be useful in the treatment of conditions involving inflammation.
Potential medicinal uses
Treatment of various conditions Due to its antioxidant and anti-inflammatory properties, 2,3-Dihydro-7-hydroxy-3-methyl-1H-inden-1-one may have potential applications in the development of new medications for treating various health conditions.
Versatility
Range of applications in different industries This chemical compound has a wide range of potential applications, making it a valuable asset in industries such as pharmaceuticals, agrochemicals, and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 40513-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,1 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40513-50:
(7*4)+(6*0)+(5*5)+(4*1)+(3*3)+(2*5)+(1*0)=76
76 % 10 = 6
So 40513-50-6 is a valid CAS Registry Number.
40513-50-6Relevant academic research and scientific papers
Concise Total Synthesis of Agarozizanol B via a Strained Photocascade Intermediate
Bach, Thorsten,Jandl, Christian,N?sborg, Line,Rauscher, Niklas
supporting information, p. 24039 - 24042 (2021/10/07)
The prezizane-type sesquiterpene agarozizanol B was synthesized employing a photochemical cascade reaction as the key step. Starting from a readily available 1-indanone with a tethered olefin, a strained tetracyclic skeleton was assembled which contained all carbon atoms of the sesquiterpene with the correct relative configuration. The conversion into the tricyclic prezizane skeleton was accomplished by a strategic cyclopropane bond cleavage. Prior to the cyclopropane ring opening an adaption of the oxidation state was required, which could be combined with a reductive resolution step. After removal of two functional groups, the natural product was obtained both in racemic form or, if resolved, as the (+)-enantiomer which was shown to be identical to the natural product.
One-step Preparation of Some Synthetically Useful Indanones
Sarkar, Asoke K.,Sinha, Nitai C.,Dutta, Lakshmi N.
, p. 1061 - 1064 (2007/10/02)
Various indanones (2a-e) have been conveniently prepared in fairly good yields from phenyl esters of α-bromobutyrates (1a-d) in one-step through the application of Fries rearrangement followed by Friedel-Craft cyclisation.
