13560-37-7 Usage
Description
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene, also known as 4'-methoxy-α-methylstilbene, is a chemical compound with the molecular formula C21H20O. It is a derivative of stilbene and is characterized as a white solid that is insoluble in water but soluble in organic solvents. 1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is known for its antioxidant and anti-inflammatory properties, as well as its potential applications in the pharmaceutical, dye, and cosmetic industries.
Uses
Used in Pharmaceutical Synthesis:
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is used as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and properties.
Used in Dye Production:
In the dye industry, 1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is used as a starting material for the production of different types of dyes, leveraging its chemical reactivity and color-producing capabilities.
Used in Organic Compounds Synthesis:
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is also utilized in the synthesis of other organic compounds, contributing to its versatility in the chemical industry.
Used in Medicinal Products:
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is used as an active ingredient in medicinal products, taking advantage of its antioxidant and anti-inflammatory properties to provide therapeutic benefits.
Used in Cosmetic Products:
In the cosmetic industry, this compound is used for its potential to improve the efficacy of products, thanks to its antioxidant and anti-inflammatory properties.
Used in Anticancer Research:
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is used as a subject of research in the field of cancer treatment, with studies indicating that it may inhibit the growth of certain cancer cells, making it a promising candidate for further investigation and potential application in oncology.
Used in Research and Development:
1-(1,1-diphenylprop-1-en-2-yl)-4-methoxybenzene is also used in research and development settings to explore its potential applications and properties further, contributing to the advancement of scientific knowledge in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 13560-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13560-37:
(7*1)+(6*3)+(5*5)+(4*6)+(3*0)+(2*3)+(1*7)=87
87 % 10 = 7
So 13560-37-7 is a valid CAS Registry Number.
13560-37-7Relevant articles and documents
Insights into the general and efficient cross McMurry reactions between ketones
Duan, Xin-Fang,Zeng, Jing,Lue, Jia-Wei,Zhang, Zhan-Bin
, p. 9873 - 9876 (2007/10/03)
The selective cross McMurry couplings of diaryl or aryl ketones with various substituted ketones were achieved in 53-94% isolated yields. It is believed that the strong affinity of the substituents to the low-valent titanium surface plays an important role in regards to moderating selectivity. Through the introduction of such substituents followed by their removal post McMurry coupling, structurally similar ketones can be effectively cross-coupled.
