57934-48-2 Usage
Furan derivative
The compound belongs to the furan derivative family, which is a group of organic compounds that contain a furan ring.
Two furan rings
The compound has two furan rings, which are five-membered rings that are oxygen-containing heterocyclic compounds.
Phenyl group
The compound contains a phenyl group, which is a six-membered carbon ring with alternating single and double bonds.
Dihydro
The compound is dihydro, meaning it contains two hydrogen atoms that are attached to the same carbon atom.
(E,E)isomerism
The compound has two double bonds that are in the E (entgegen) configuration, meaning they are on the opposite side of the molecule.
Potential applications
The compound has potential applications in the field of organic chemistry and material science, as well as possible biological or pharmaceutical applications due to its structural features.
Further research needed
Further research and investigation are required to fully understand the properties and potential uses of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 57934-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,3 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57934-48:
(7*5)+(6*7)+(5*9)+(4*3)+(3*4)+(2*4)+(1*8)=162
162 % 10 = 2
So 57934-48-2 is a valid CAS Registry Number.
57934-48-2Relevant academic research and scientific papers
Synthesis of 1,4-diphenylbutadiene derivatives: Novel inducer of tissue-type plasminogen activator (t-PA) in cultured bovine endothelial cells
Sai, Hiroshi,Ogiku, Tsuyoshi,Ohmizu, Hiroshi,Ohtani, Akio
, p. 1686 - 1693 (2007/10/03)
(E,E)-1,4-Diphenylbutadiene derivatives were synthesized by utilizing the Stobbe reaction of dimethyl succinate as a key step. Their stereoisomers were also synthesized stereoselectively by means of the cross-coupling reaction of the vinylstannanes and the vinylbromides, which were obtained from the propiolic acid esters by stereoselective hydrostannation, as a key step. To discover novel stimulators of fibrinolysis in vascular endothelial cells, the synthesized compounds were added to cultured bovine endothelial cells to determine the activity of the plasminogen activator in the conditioned medium. Of the synthesized compounds, three compounds were found to stimulate the activity of the plasminogen activator in endothelial cells. In addtition, these compounds inhibited thrombus formation in a rat model of venous thrombosis.
