5111-70-6 Usage
Description
5-Methoxy-1-indanone is a white to light yellow crystal powder with cytotoxic potential, which has been assessed for its potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
5-Methoxy-1-indanone is used as a pharmaceutical compound for its cytotoxic properties. It is being investigated for its potential to target and inhibit the growth of cancer cells, making it a promising candidate for the development of new anticancer drugs.
Used in Chemical Synthesis:
5-Methoxy-1-indanone is used as a key intermediate in the synthesis of various organic compounds. Its unique chemical structure allows it to be a versatile building block for the creation of a wide range of molecules with different applications in the chemical, pharmaceutical, and materials science industries.
Used in Flavor and Fragrance Industry:
5-Methoxy-1-indanone, due to its distinct chemical properties, can be used as a component in the development of novel fragrances and flavors. Its unique scent profile can contribute to the creation of new and innovative products in the perfumery and flavor industries.
Used in Research and Development:
5-Methoxy-1-indanone is used as a research compound for studying its cytotoxic effects and potential applications in various fields. Scientists and researchers can utilize this compound to conduct experiments and develop new methodologies for drug discovery, material synthesis, and other scientific applications.
Used in Material Science:
5-Methoxy-1-indanone can be used as a component in the development of new materials with specific properties. Its unique chemical structure can be exploited to create materials with enhanced properties, such as improved stability, reactivity, or selectivity, which can be applied in various industries, including electronics, coatings, and adhesives.
Synthesis Reference(s)
Journal of the American Chemical Society, 106, p. 2469, 1984 DOI: 10.1021/ja00320a060The Journal of Organic Chemistry, 35, p. 647, 1970 DOI: 10.1021/jo00828a022Tetrahedron Letters, 8, p. 2763, 1967
Check Digit Verification of cas no
The CAS Registry Mumber 5111-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5111-70:
(6*5)+(5*1)+(4*1)+(3*1)+(2*7)+(1*0)=56
56 % 10 = 6
So 5111-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-12-8-3-4-9-7(6-8)2-5-10(9)11/h3-4,6H,2,5H2,1H3
5111-70-6Relevant articles and documents
Facile transformation of benzocyclobutenones into 2,3-benzodiazepines via 4π-8π tandem electrocyclic reactions involving net insertion of diazomethylene compounds
Matsuya, Yuji,Ohsawa, Noriko,Nemoto, Hideo
, p. 13072 - 13073 (2006)
Efficient transformations of benzocyclobutenones into 2,3-benzodiazepines by a formal insertion of diazomethylene compounds are described. This sequential process includes nucleophilic addition of diazomethylene anion, oxy-anion accelerated o-quinodimethane formation by an electrocyclic ring-opening reaction, and 8π-electrocyclization in one-pot under remarkably mild conditions. Intermediary oxy-anion plays an important role for the efficient transformations. Copyright
Electrochemical Difunctionalization of Styrenes via Chemoselective Oxo-Azidation or Oxo-Hydroxyphthalimidation
Jiang, Haobin,Wang, Feng,Ye, Zenghui,Zhang, Fengzhi,Zhu, Rongjin
supporting information, p. 8240 - 8245 (2021/11/17)
Atom- and step-economic oxo-azidation and oxo-hydroxyphthalimidation of styrenes have been developed under mild electrolytic conditions, respectively. Various valuable alpha-azido or hydroxyphthalimide aromatic ketones were synthesized efficiently from readily available styrenes, azides, and N-hydroxyphthalimides. Mechanism studies show that two different pathways involved in these two transformations.
Synthesis of diaryl ketones through oxidative cleavage of the C-C double bonds in N -Sulfonyl enamides
Kim, Hyunseok,Park, Sangjune,Baek, Yonghyeon,Um, Kyusik,Han, Gi Uk,Jeon, Da-Hye,Han, Sang Hoon,Lee, Phil Ho
, p. 3486 - 3496 (2018/04/14)
An oxidative cleavage of a C-C double bond is developed from the photochemical [2+2]-cycloaddition of diaryl N-tosyl enamides, aryl heteroaryl N-tosyl enamides, and N-tosyl cyclic enamides with singlet molecular oxygen, followed by a ring-opening reaction mediated by Cs2CO3 under air and sunlight without the use of photosesitizer, producing symmetrical and unsymmetrical diaryl, heterodiaryl, and cyclic ketones in good to excellent yields. Moreover, the oxidative cleavage of C-C triple bonds from 1-alkynes is demonstrated for the synthesis of symmetrical and unsymmetrical ketones from the Cu-catalyzed [3+2]-cycloaddition, Rh-catalyzed alkoxyarylation, photooxygenation, and ring-opening reaction in one-pot. Because the synthesis of the symmetrical and unsymmetrical diaryl and/or heterodiaryl ketones bearing an electron-donating group is not easy, the present method is notable.
