104761-62-8 Usage
Molecular structure
A complex structure containing a fluorine-substituted tetrahydronaphthalene group and an ethylbenzene unit.
Classification
A benzoic acid derivative.
Fluorine substitution
Presence of a fluorine atom in the tetrahydronaphthalene group, which can influence the compound's reactivity and properties.
Ethylbenzene unit
A part of the molecule that consists of an ethyl group attached to a benzene ring, which can affect the compound's solubility and stability.
Potential applications
Organic synthesis, pharmaceuticals, and materials science.
Physical properties
May exhibit various physical properties, such as solubility, melting point, and boiling point, which can be important for its use in different applications.
Chemical properties
Reactivity, stability, and other chemical properties that can determine its suitability for specific applications.
Biological activity
The compound may have potential biological activity, which could make it useful in pharmaceuticals or other research areas.
Further studies needed
More research and evaluations are required to fully understand the characteristics and potential uses of 2-[1-(3-fluoro-5,6,7,8-tetrahydronaphthalen-2-yl)ethyl]benzoic acid.
Check Digit Verification of cas no
The CAS Registry Mumber 104761-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104761-62:
(8*1)+(7*0)+(6*4)+(5*7)+(4*6)+(3*1)+(2*6)+(1*2)=108
108 % 10 = 8
So 104761-62-8 is a valid CAS Registry Number.
104761-62-8Relevant articles and documents
The 5-, 6-, and 10-Fluoro-1,2,3,4-tetrahydro-7,12-dimethylbenzanthracenes. Comparative Acid-Catalyzed Isomerization to Exo Methylene Tautomers: A 6-Fluoro Peri Effect
Witiak, Donald T.,Abood, Norman A.,Goswami, Shyamaprosad,Milo, George E.
, p. 4499 - 4507 (2007/10/02)
Syntheses for 5-, 6-, and 10-fluoro-1,2,3,4-tetrahydro-7,12-dimethylbenzanthracenes (3-5) from an aminotetralin-HCl 6, fluorotetralin 14, and tetrahydronaphthaldehyde 29, respectively, are described.Comparative acid-catalyzed isomerization studies in refluxing benzene revealed that the 6-F analogue 4 equilibrates with 12- and 7-methylene tautomers 20 and 21 within 1 h.When the 12-methylene tautomer 20 was treated with p-toluenesulfonic acid in refluxing benzene the thermodynamic product ratio (4/20/21 = 1.0:0.6:2.8) was obtained after 72 h.These data are markedlydifferent than results observed for acid-catalyzed isomerization of 1,2,3,4-tetrahydro-7,12-dimethylbenzanthracene (TH-DMBA, 1), 5F-TH-DMBA (3) or 10F-TH-DMBA (5) which after 72 h only afforded aryl to 7-methylene isomer ratios of 14:1, 8:1 and 8:1, respectively.The additional peri interaction between the 7-CH3 and 6-F functions of 4 serves as explanation for the facile acid-catalyzed isomerization of 4 to the sterically least crowded, thermodynamically more stable 7-methylene tautomer 21.
