2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid is a complex organic compound characterized by a naphthalene ring, which is a fused ring system consisting of two benzene rings. 2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid features a carboxylic acid group at the 1-position of the naphthalene, which provides it with acidic properties. Additionally, it has a thiophene ring (a five-membered ring with one sulfur atom) attached to the 2-position of the naphthalene through a carbonyl group, forming a thiophen-2-ylcarbonyl moiety. This structure endows the molecule with unique electronic and steric properties, making it a potentially interesting candidate for various chemical and pharmaceutical applications, such as in the synthesis of novel compounds with specific biological activities or material properties.
7495-40-1
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Basic information
- Product Name: 2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid
- Synonyms:
- CAS NO:7495-40-1
- Molecular Formula: C16H10O3S
- Molecular Weight: 282.3138
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 545.1°C at 760 mmHg
- Flash Point: 283.5°C
- Appearance: N/A
- Density: 1.386g/cm3
- Vapor Pressure: 1.03E-12mmHg at 25°C
- Refractive Index: 1.705
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid(7495-40-1)
- EPA Substance Registry System: 2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid(7495-40-1)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 7495-40-1(Hazardous Substances Data)
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7495-40-1 Usage
Derivative of naphthalene
A modified version of the naphthalene molecule, which is a fused bicyclic aromatic compound.Contains a carbonyl group
A functional group consisting of a carbon atom double-bonded to an oxygen atom (C=O).Attached to a thiophene ring
The carbonyl group is connected to a five-membered ring containing sulfur, which is a heterocyclic aromatic compound.Potential applications in organic chemistry
2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid may be used as a building block or intermediate in the synthesis of more complex organic molecules.Potential applications in drug development
The unique structure and properties of this chemical compound may lead to the discovery of new biological activities, making it a potential candidate for drug development.Exhibiting biological activities
2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid may interact with biological systems, potentially leading to therapeutic effects or other biological functions.Research insights
Further investigation into the properties, reactivity, and potential uses of this chemical compound can provide valuable information for various fields, such as pharmaceuticals, materials science, and environmental science.Check Digit Verification of cas no
The CAS Registry Mumber 7495-40-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.Calculate Digit Verification of CAS Registry Number 7495-40:
(6*7)+(5*4)+(4*9)+(3*5)+(2*4)+(1*0)=121
121 % 10 = 1
So 7495-40-1 is a valid CAS Registry Number.
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7495-40-1Downstream Products
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2-(thiophen-2-ylcarbonyl)naphthalene-1-carboxylic acid
