13621-25-5 Usage
Description
5,7-Dimethyl-1-tetralone is an organic compound characterized by its unique molecular structure, featuring two methyl groups at the 5th and 7th positions of the tetralone backbone. 5,7-Dimethyl-1-tetralone is known for its potential applications in various chemical and pharmaceutical processes due to its versatile chemical properties.
Uses
Used in Pharmaceutical Industry:
5,7-Dimethyl-1-tetralone is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
5,7-Dimethyl-1-tetralone is used as a starting material for the synthesis of new coumarin derivatives. These derivatives have a wide range of applications, including their use as pharmaceuticals, agrochemicals, and dyes.
Used in Organic Chemistry:
5,7-Dimethyl-1-tetralone is used as a reactant in the synthesis of 5,7-dimethyl-1,2-naphthoquinones through a microwave-assisted selenium dioxide oxidation reaction. This process demonstrates the compound's utility in organic chemistry for the production of complex molecular structures with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13621-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,2 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13621-25:
(7*1)+(6*3)+(5*6)+(4*2)+(3*1)+(2*2)+(1*5)=75
75 % 10 = 5
So 13621-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O/c1-8-6-9(2)10-4-3-5-12(13)11(10)7-8/h6-7H,3-5H2,1-2H3
13621-25-5Relevant articles and documents
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Mosby
, p. 485,488 (1953)
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Evans,Smith
, p. 798 (1954)
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An Electrophilic Trifluoromethylthiolation of Silylenol Ethers and β-Naphthols with Diethylaminosulfur Trifluoride and (Trifluoromethyl)trimethylsilane
Saravanan, Perumal,Anbarasan, Pazhamalai
, p. 2894 - 2899 (2018/08/17)
An efficient and general trifluoromethylthiolation of silylenol ethers and β-naphthols have been accomplished employing the combination of diethylaminosulfur trifluoride (DAST) and (trifluoromethyl)trimethylsilane (CF3TMS) as source of electrophilic trifluoromethylthio moiety for the synthesis of α-trifluoromethylthiolated carbonyl compounds and β-naphthols in good yields. Important features of this method include wide functional group tolerance and use of readily available DAST/CF3TMS. Potential of the methodology was demonstrated via the synthesis of α-trifluoromethylthiolated (+)-4-cholesten-3-one and naphthoquinone. (Figure presented.).
Sustainable flow oppenauer oxidation of secondary benzylic alcohols with a heterogeneous zirconia catalyst
Chorghade, Rajeev,Battilocchio, Claudio,Hawkins, Joel M.,Ley, Steven V.
supporting information, p. 5698 - 5701 (2013/12/04)
A flow chemistry process for the Oppenauer oxidation of benzylic secondary alcohols using partially hydrated zirconium oxide and a simple carbonyl containing oxidant such as acetone, cyclohexanone, and neopentanal is reported. The heterogeneous oxidative system could be applied to a wide range of functionalized alcohol substrates, allowing clean and fast delivery of ketone products within a few minutes between 40 and 100 C.
