846023-34-5 Usage
Molecular Weight
503.74 g/mol
Properties
1. Functional Groups:
Amide ( -\textCONH2 )
Cyano ( -\textCN )
Chloro ( -\textCl )
Methoxy ( -\textOCH3 )
2. Molecular Weight: 503.74 g/mol
3. Physical State: Not specified (requires experimental determination)
4. Solubility: May vary depending on the solvent due to the presence of different functional groups.
5. Potential Applications:
Pharmaceuticals: The compound's unique structure and functional groups may offer opportunities for drug design and development.
Materials Science: It could be utilized in the synthesis of materials with specific properties.
Organic Chemistry: Valuable in organic synthesis for creating novel compounds and studying reaction mechanisms.
6. Reactivity: Reactivity may vary depending on the specific functional groups and their positions within the molecule.
7. Toxicity: Requires further investigation to determine potential toxicity and safety considerations.
8. Stability: Stability under various conditions needs to be evaluated to assess its shelf life and storage requirements.
9. Biological Activity: Potential biological activities, such as pharmacological effects, need to be studied to understand its potential medicinal properties.
10. Structural Complexity: The compound's complex structure suggests the possibility of diverse chemical reactions and interactions.
11. Analytical Characterization: Techniques such as spectroscopy and chromatography can be employed for detailed structural analysis.
12. Potential for Modification: The compound may serve as a precursor for the synthesis of derivatives with tailored properties for specific applications.
13. Regulatory Considerations: Regulatory compliance and safety assessments are necessary before any potential commercial applications.
14. Further Research Needs: Comprehensive studies are required to explore its full range of properties and potential applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 846023-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,6,0,2 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 846023-34:
(8*8)+(7*4)+(6*6)+(5*0)+(4*2)+(3*3)+(2*3)+(1*4)=155
155 % 10 = 5
So 846023-34-5 is a valid CAS Registry Number.
846023-34-5Relevant academic research and scientific papers
Process for preparation of 4-amino-3-quinolinecarbonitriles
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Page/Page column 8, (2010/02/10)
This invention discloses a process for the preparation of a 4-amino-3-quinolinecarbonitrile comprising combining an amine compound with a cyanoacetic acid and an acid catalyst to yield a cyanoacetamide; condensing the cyanoacetamide with an optionally up to tetra-substituted aniline in an alcoholic solvent and a trialkylorthoformate to yield a 3-amino-2-cyanoacrylamide; combining the 3-amino-2-cyanoacrylamide with phosphorus oxychloride in acetonitrile, butyronitrile, toluene or xylene, optionally in the presence of a catalyst to yield a 4-amino-3-quinolinecarbonitrile and also discloses a process for the preparation of a 7-amino-thieno[3,2-b]pyridine-6-carbonitrile comprising combining a disubstituted 3-amino thiophene with a cyanoacetamide and trialkylorthoformate in an alcoholic solvent to obtain a 3-amino-2-cyanoacrylamide; and combining the 3-amino-2-cyanoacrylamide with phosphorus oxychloride and acetonitrile, butyronitrile, toluene or xylene, optionally in the presence of a catalyst to yield a 7-amino-thieno[3,2-b]pyridine-6-carbonitrile and also discloses a process for the preparation of a 4-amino-3-quinolinecarbonitrile by combining an amine compound with a cyanoacetic acid and a peptide coupling reagent to obtain a suspension; filtering the suspension to yield a cyanoacetamide; condensing the cyanoacetamide with an optionally up to tetra-substituted aniline, an alcoholic solvent, and triethylorthoformate to yield a 3-amino-2-cyanoacrylamide; and combining the 3-amino-2-cyanoacrylamide with phosphorus oxychloride to yield a 4-amino-3-quinolinecarbonitrile.
