2700-47-2 Usage
Description
6'-Methoxy-2'-propiononaphthone is an organic compound that serves as a valuable building block in the field of organic synthesis. It is characterized by its molecular structure, which includes a naphthone core with a methoxy group at the 6' position and a propionyl group at the 2' position. 6'-Methoxy-2'-propiononaphthone has been reported to have a specific density, making it a useful component in various chemical reactions and applications.
Uses
Used in Pharmaceutical Industry:
6'-Methoxy-2'-propiononaphthone is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, such as those targeting specific diseases or conditions.
Used in Fragrance Industry:
6'-Methoxy-2'-propiononaphthone is used as a fragrance ingredient in the creation of various scented products, such as perfumes, colognes, and other personal care items. Its distinct chemical structure contributes to the overall aroma profile of these products, providing a unique and desirable scent.
Used in Chemical Research:
6'-Methoxy-2'-propiononaphthone is used as a research compound in the field of organic chemistry. It serves as a starting material for the synthesis of more complex molecules and can be used to study various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge in this area.
Used in Dye and Pigment Industry:
6'-Methoxy-2'-propiononaphthone is used as a precursor in the production of dyes and pigments. Its chemical properties make it suitable for the development of new colorants with specific characteristics, such as improved stability, color intensity, or application properties.
Used in Material Science:
6'-Methoxy-2'-propiononaphthone can be used in the development of new materials with specific properties, such as improved conductivity, mechanical strength, or thermal stability. Its unique structure allows for the creation of novel materials with potential applications in various industries, including electronics, aerospace, and automotive.
Synthesis Reference(s)
Synthetic Communications, 20, p. 383, 1990 DOI: 10.1080/00397919008052779
Check Digit Verification of cas no
The CAS Registry Mumber 2700-47-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2700-47:
(6*2)+(5*7)+(4*0)+(3*0)+(2*4)+(1*7)=62
62 % 10 = 2
So 2700-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-9(14)10-3-4-12-8-13(15-2)6-5-11(12)7-10/h3-8H,1-2H3
2700-47-2Relevant articles and documents
Jacques et al.
, p. 150,161 (1960)
Synthesis method of D,L-naproxen
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Paragraph 0047-0050, (2019/10/01)
The invention provides a synthesis method of D,L-naproxen. The synthesis method is characterized by comprising the step of removing bromine: taking D,L-2-(5-bromo-6-methoxyl-naphthyl)-sodium propionate as a raw material, and taking water and dioxane as solvents, adding a catalyst under alkaline conditions and nitrogen protection, reacting under 80-90 DEG C, filtering after the reaction is completed, and regulating the pH (Potential of hydrogen) of filtrate by acid to obtain a final product, wherein the catalyst is one of tetrakis(triphenylphosphine)palladium or diacetatobis(triphenylphosphine)palladium(II) or palladium chloride taking triphenylphosphine as a ligand. According to the synthesis method, through optimizing the synthesis method of naproxen, the tetrakis(triphenylphosphine)palladium and the diacetatobis(triphenylphosphine) palladium(II) as well as the palladium chloride taking the triphenylphosphine as the ligand are adopted as the catalyst to remove the bromine on a benzene ring; hydrogenation and high pressure are not needed; the reaction is safe and reliable; the yield is high; the synthesis method is suitable for industrial production.
Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents
Malmedy, Florence,Wirth, Thomas
supporting information, p. 16072 - 16077 (2016/10/30)
The first stereoselective version of an iodine(III)-mediated rearrangement of arylketones in the presence of orthoesters is described. The reaction products, α-arylated esters, are very useful intermediates in the synthesis of bioactive compounds such as ibuprofen. With chiral lactic acid-based iodine(III) reagents product selectivities of up to 73 % ee have been achieved.
