85666-05-3 Usage
General Description
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is a chemical compound with a molecular structure of C13H9NO. It is a phenolic compound with a pyridine ring and a vinyl group attached to a phenol group. (E)-4-(2-(pyridin-3-yl)vinyl)phenol has demonstrated potential biological activities, including antioxidant and anti-inflammatory properties. It has also been studied for its potential application in the development of pharmaceutical drugs, particularly for the treatment of conditions such as cancer and inflammation. Additionally, it has been investigated for its potential use in materials science, particularly in the development of organic electronic devices due to its unique molecular structure and electronic properties.
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
