7498-69-3 Usage
Description
(2E)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enoic acid is a chemical compound with the molecular formula C15H16O2. It is a derivative of tetrahydronaphthalene and features a propenoic acid functional group. (2E)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enoic acid is recognized for its potential pharmaceutical properties and is often utilized in organic and medicinal chemistry.
Uses
Used in Pharmaceutical Development:
(2E)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential therapeutic effects. It is particularly considered for the development of drugs targeting neurological disorders and inflammation-related conditions due to its unique structural features and chemical properties.
Used in Organic Chemistry Research:
In the field of organic chemistry, (2E)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enoic acid serves as a valuable compound for studying reaction mechanisms and exploring new synthetic pathways. Its reactivity and structural attributes make it a subject of interest for creating novel organic molecules with potential applications in various industries.
The specific properties and potential uses of (2E)-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enoic acid continue to be the focus of ongoing research and exploration within the scientific community, as its full range of applications and therapeutic potential are yet to be fully understood and realized.
Check Digit Verification of cas no
The CAS Registry Mumber 7498-69-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7498-69:
(6*7)+(5*4)+(4*9)+(3*8)+(2*6)+(1*9)=143
143 % 10 = 3
So 7498-69-3 is a valid CAS Registry Number.
7498-69-3Relevant articles and documents
Aromatic Spiranes, XVI: Syntheses of Mono- and Dianellated 2,2'-Spirobiindane-1,1'diones
Neudeck, Horst K.
, p. 597 - 622 (2007/10/02)
The spiroketones 19, 21, 24, 27, and 31 were prepared by cyclisation of the dicarboxylic acids and their acid chlorides, resp., (18, 20, 22, 23, 25, 26, 28, and 30) with polyphosphoric acid (PPA) or SnCl4.The latter compounds were synthesized by alkylation of the appropriate β-keto esters 10, 11, 12, and 13 with the "benzyl chlorides" 14, 15, 16, and subsequent retro-Claisen reaction.The spiro compounds 21a and 39 were obtained by PPA-cyclisation of the keto acids 35 and 38, which in turn were prepared by aldol-reaction of the ketones s-hydrindacen-1-on and 9a with phthalaldehydic acid to the olefinic keto acids 33 and 36 followed by catalytic hydrogenation. - Keywords: Indane-1-one; s-Hydrindacene-1-one; Tetrahydrobenzoindane-1-one; β-Keto esters; Phthalaldehydic acid; Spiro cyclisation; 2,2'-Spirobiindane-1,1'-diones; 1H-nmr spectra; Mass spectra
