85666-05-3 Usage
Description
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is a phenolic compound characterized by a molecular structure of C13H9NO. It features a pyridine ring and a vinyl group attached to a phenol group, which endows it with unique chemical and electronic properties. (E)-4-(2-(pyridin-3-yl)vinyl)phenol has shown potential biological activities, such as antioxidant and anti-inflammatory properties, and has been explored for its application in pharmaceutical drugs for treating cancer and inflammation. Furthermore, its molecular structure and electronic properties have made it a candidate for use in materials science, particularly in the development of organic electronic devices.
Uses
Used in Pharmaceutical Industry:
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is used as a potential therapeutic agent for the treatment of cancer and inflammation. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of pharmaceutical drugs targeting these conditions.
Used in Materials Science:
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is used as a component in the development of organic electronic devices. Its unique molecular structure and electronic properties contribute to its potential application in this field, where it may be utilized to enhance the performance of such devices.
Check Digit Verification of cas no
The CAS Registry Mumber 85666-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,6 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85666-05:
(7*8)+(6*5)+(5*6)+(4*6)+(3*6)+(2*0)+(1*5)=163
163 % 10 = 3
So 85666-05-3 is a valid CAS Registry Number.
85666-05-3Relevant articles and documents
Tandem heck/decarboxylation/heck strategy: Protecting-group-free synthesis of symmetric and unsymmetric hydroxylated stilbenoids
Shard, Amit,Sharma, Naina,Bharti, Richa,Dadhwal, Sumit,Kumar, Rajesh,Sinha, Arun K.
supporting information, p. 12250 - 12253 (2013/02/22)
Ride the (micro)wave: The title strategy has been developed for the synthesis of various symmetric or unsymmetric hydroxylated stilbenoids utilizing 4-halophenols and acrylic acid as coupling partners (see scheme; DMA=N,N-dimethylacetamide, MW=microwave). Protecting groups are not necessary and a single palladium catalyst is used. Copyright
Antiinflammatory 2,6-Di-tert-butyl-4-(2-arylethenyl)phenols
Lazer, Edward S.,Wong, Hin-Chor,Possanza, Genus J.,Graham, Anne G.,Farina, Peter R.
, p. 100 - 104 (2007/10/02)
A series of 2,6-di-tert-butyl-4-(2-arylethenyl)phenols was prepared and examined for their ability to inhibit cyclooxygenase and 5-lipoxygenase in vitro and developing adjuvant arthritis in vivo in the rat.Structure-activity relationships are discussed.Am
