68684-63-9 Usage
Description
1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene is a chemical compound characterized by a molecular structure that features a hydroxyphenyl group attached to a diphenylbutene moiety. 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene is classified as a substituted stilbene, which implies a central stilbene core with a hydroxyphenyl group at one end. Its unique chemical structure and properties suggest potential applications across various sectors such as pharmaceuticals, dyes, and materials science.
Uses
Used in Pharmaceutical Industry:
1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure may allow it to interact with specific biological targets, potentially leading to the development of new drugs or therapies.
Used in Dye Industry:
In the dye industry, 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene is used as a chemical intermediate for the synthesis of various dyes. Its distinct chemical properties may contribute to the creation of novel dyes with specific color characteristics or improved stability.
Used in Materials Science:
1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene is utilized as a component in the development of advanced materials. Its incorporation into materials may enhance their properties, such as optical, electronic, or mechanical characteristics, for use in various applications, including electronics, sensors, or coatings.
Please note that the specific applications and reasons for using 1-(4-hydroxyphenyl)-1,2-diphenyl-1-butene in each industry are hypothetical and based on the general properties of substituted stilbene compounds. Further research and development would be required to confirm these potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 68684-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,8 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68684-63:
(7*6)+(6*8)+(5*6)+(4*8)+(3*4)+(2*6)+(1*3)=179
179 % 10 = 9
So 68684-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H20O/c1-2-21(17-9-5-3-6-10-17)22(18-11-7-4-8-12-18)19-13-15-20(23)16-14-19/h3-16,23H,2H2,1H3/b22-21+
68684-63-9Relevant articles and documents
Peroxidase-mediated dealkylation of tamoxifen, detected by electrospray ionization-mass spectrometry, and activation to form DNA adducts
Gaikwad, Nilesh W.,Bodell, William J.
, p. 340 - 347 (2012)
Tamoxifen (TAM) is extensively used for the treatment and prevention of breast cancer. Associated with TAM treatment is a two- to eightfold increase in risk of endometrial cancer. To understand the mechanisms associated with this increased risk several pa
Design and synthesis of norendoxifen analogues with dual aromatase inhibitory and estrogen receptor modulatory activities
Lv, Wei,Liu, Jinzhong,Skaar, Todd C.,Flockhart, David A.,Cushman, Mark
, p. 2623 - 2648 (2015/04/14)
Both selective estrogen receptor modulators and aromatase inhibitors are widely used for the treatment of breast cancer. Compounds with both aromatase inhibitory and estrogen receptor modulatory activities could have special advantages for treatment of br
Direct copper-catalyzed α-arylation of benzyl phenyl ketones with aryl iodides: Route towards tamoxifen
Danoun, Grégory,Tlili, Anis,Monnier, Florian,Taillefer, Marc
supporting information, p. 12815 - 12819 (2013/02/22)
No activation needed: The first efficient method for direct α-arylation of non-activated or non-protected family of enolizable ketones with simple aryl iodides employs a catalytic copper system. The method shows potential for the easy and step-economical synthesis of tamoxifen, the most commonly administrated drug for the management of breast cancer. R, R′, R′′ = electron-donating or electron-withdrawing groups. Copyright
