89998-98-1 Usage
Explanation
The compound consists of 25 carbon atoms, 18 hydrogen atoms, and 1 oxygen atom.
Explanation
The compound contains a five-membered benzofuran ring (a fused benzene and furan ring) and a diphenylethenyl group (two phenyl groups connected by a vinylene bridge).
3. Synthetic organic compound
Explanation
It is a man-made chemical compound, not found naturally in the environment.
4. Use as a reactant in organic chemistry
Explanation
Due to its unique structure, 2-[(E)-1,2-diphenylethenyl]-1-benzofuran can participate in various chemical reactions, making it a valuable reactant in organic synthesis.
5. Building block for complex organic molecules
Explanation
The compound can be used as a starting material to create more complex organic molecules, expanding its utility in organic chemistry.
6. Potential pharmacological properties
Chemical structure
Benzofuran ring and diphenylethenyl group
Check Digit Verification of cas no
The CAS Registry Mumber 89998-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,9 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89998-98:
(7*8)+(6*9)+(5*9)+(4*9)+(3*8)+(2*9)+(1*8)=241
241 % 10 = 1
So 89998-98-1 is a valid CAS Registry Number.
89998-98-1Relevant articles and documents
A simple, multidimensional approach to high-throughput discovery of catalytic reactions
Robbins, Daniel W.,Hartwig, John F.
scheme or table, p. 1423 - 1427 (2012/01/03)
Transition metal complexes catalyze many important reactions that are employed in medicine, materials science, and energy production. Although high-throughput methods for the discovery of catalysts that would mirror related approaches for the discovery of medicinally active compounds have been the focus of much attention, these methods have not been sufficiently general or accessible to typical synthetic laboratories to be adopted widely. We report a method to evaluate a broad range of catalysts for potential coupling reactions with the use of simple laboratory equipment. Specifically, we screen an array of catalysts and ligands with a diverse mixture of substrates and then use mass spectrometry to identify reaction products that, by design, exceed the mass of any single substrate. With this method, we discovered a copper-catalyzed alkyne hydroamination and two nickel-catalyzed hydroarylation reactions, each of which displays excellent functional-group tolerance.
