845873-35-0 Usage
Properties
1. Chemical Formula: \textC14\textH17\textBO2\textS
2. Molecular Weight: Approximately 261.16 g/mol
3. Structural Features: Contains a thiophene ring, an aldehyde functional group, and a boron-containing substituent.
4. Physical State: Typically a solid at room temperature, but can vary depending on its form (e.g., powder, crystalline).
5. Solubility: Soluble in some organic solvents like dichloromethane, tetrahydrofuran, and toluene.
6. Reactivity: Exhibits reactivity typical of aldehydes and boron-containing compounds, participating in various organic reactions.
Specific Content
1. Thiophene Derivative: The compound contains a thiophene ring, a five-membered heterocycle consisting of four carbon atoms and one sulfur atom. Thiophene derivatives often exhibit interesting electronic properties.
2. Boron-Containing Substituent: Contains a boron atom incorporated into the molecule, specifically in the form of a boron-oxygen-heterocycle. Boron-containing compounds are widely used in organic synthesis due to their unique reactivity and versatility.
3. Aldehyde Functional Group: Features an aldehyde functional group ( -\textCHO ), which is highly reactive and participates in various organic reactions such as nucleophilic addition and oxidation.
4. Versatile Reagent: Widely utilized in organic synthesis and materials science due to its versatility in forming carbon-carbon and carbon-heteroatom bonds.
5. Building Block: Serves as a crucial building block for the synthesis of various organic compounds and materials.
6. Applications:
Pharmaceuticals: Used in the synthesis of pharmaceutical compounds due to its ability to form complex molecular structures.
Agrochemicals: Employed in the production of agrochemicals for agricultural applications.
Materials Science: Utilized in the development of materials with potential applications in optoelectronic devices and organic electronics.
Organic Synthesis: Plays a significant role in the construction of complex organic molecules with desired properties.
Overall, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde is a versatile compound with diverse applications in organic synthesis and materials science, owing to its unique structural features and reactivity profile.
Check Digit Verification of cas no
The CAS Registry Mumber 845873-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 845873-35:
(8*8)+(7*4)+(6*5)+(5*8)+(4*7)+(3*3)+(2*3)+(1*5)=210
210 % 10 = 0
So 845873-35-0 is a valid CAS Registry Number.
845873-35-0Relevant academic research and scientific papers
Jhang, Yuan-Ye,Fan-Chiang, Tai-Ting,Huang, Jun-Min,Hsieh, Jen-Chieh
, p. 1154 - 1157 (2016)
A novel procedure for the Cu-catalyzed systematic synthesis of phenanthridinium bromide is reported. This transformation was achieved with direct construction of central pyridinium core by using an in situ formed biaryl imine as a substrate. Tolerance of a very wide variety of N-substituents is indicated; this has never previously been disclosed by other reports. Application of this method to synthesis of the natural alkaloid bicolorine, and its derivatives, was also carried out in only three synthetic steps from commercially available compounds.
