2782-23-2 Usage
Chemical class
Aromatic hydrocarbon
Explanation
It consists of two benzene rings connected by a single bond.
Explanation
The compound's alternative name, which provides information about its structure.
Explanation
The compound is utilized in various industries for creating different products.
Explanation
It serves as a base for creating more complex and valuable compounds.
Explanation
The compound may be used to develop new materials with unique electronic properties or applications.
Explanation
This describes the specific arrangement of atoms and functional groups in the molecule.
Explanation
Most organic compounds with similar structures and molecular weights are solids at room temperature.
Explanation
Aromatic hydrocarbons with functional groups are generally soluble in organic solvents.
Explanation
The compound is expected to be stable at room temperature but could undergo reactions under certain conditions.
Explanation
The compound's toxicity is not specified, but it is important to follow safety precautions when handling chemicals with unknown toxicity.
Common uses
Production of chemicals, materials, pharmaceuticals, dyes, and polymers
Application in organic synthesis
Starting material for specialty and fine chemicals
Potential use in electronics
Building block for new compounds
Structure
Two benzene rings connected by a single bond, with an ethenyl group at the 4-position and a methoxy group at the 4'-position
Physical properties
Unknown, but likely solid at room temperature due to its molecular size and complexity
Solubility
Likely soluble in organic solvents such as ethanol, methanol, or acetone
Stability
Stable under normal conditions, but may react with strong acids, bases, or oxidizing agents
Toxicity
Unknown, but should be handled with care due to its potential effects on human health and the environment
Check Digit Verification of cas no
The CAS Registry Mumber 2782-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2782-23:
(6*2)+(5*7)+(4*8)+(3*2)+(2*2)+(1*3)=92
92 % 10 = 2
So 2782-23-2 is a valid CAS Registry Number.
2782-23-2Relevant articles and documents
Highly chemoselective cobalt-catalyzed biaryl coupling reactions
Guelak, Samet,Stepanek, Ondrej,Malberg, Jennifer,Rad, Babak Rezaei,Kotora, Martin,Wolf, Robert,Jacobi Von Wangelin, Axel
, p. 776 - 784 (2013/03/28)
A practical cobalt-catalyzed hetero-biaryl coupling reaction between aryl chlorides and arylmagnesium halides with unprecedented selectivity has been developed. The protocol utilizes 1 mol% of cheap Co(acac)3 as pre-catalyst and effects clean reactions of deactivated chlorostyrenes with only 1.1 equiv. of the Grignard reagent under mild conditions (30 °C, 5-30 min). Highly chemoselective reactions were realized even in the presence of activated bromoarenes. The olefin substituent facilitates the activation of the C-Cl bond by coordination to the catalyst. Kinetic studies indicate the operation of an arylcobaltate(i) catalyst species. Catalyst formation during the induction period was studied in the presence of cobalt(iii), (i), and (-i) pre-catalysts. The Royal Society of Chemistry 2013.
A general synthesis of diarylketones by means of a three-component cross-coupling of aryl and heteroaryl bromides, carbon monoxide, and boronic acids
Neumann, Helfried,Brennfuehrer, Anne,Beller, Matthias
experimental part, p. 3645 - 3652 (2009/04/11)
Pd(OAc)2/di-1-adamantyl-n-butylphosphine (cataCXium A) is highly active in the three-component Suzuki carbonylation and represents the most general catalyst system reported up to now. A broad range of aryl/heteroaryl bromides and aryl boronic acids can be coupled to the corresponding diarylketones at low catalyst loadings.
