CAS No.: | 83-33-0 |
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Formula: | C9h8o |
EINECS: | 201-470-1 |
Classification: | Organic Analytical Reagents |
Grade: | AR |
Specific Usage: | For Biological Purpose |
Customization: |
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Common Name | 1-Indanone | ||
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CAS Number | 83-33-0 | Molecular Weight | 132.16 |
Density | 1.1±0.1 g/cm3 | Boiling Point | 244.0±0.0 °C at 760 mmHg |
Molecular Formula | C9H8O | Melting Point | 38-40 °C(lit.) |
MSDS | ChineseUSA | Flash Point | 111.7±0.0 °C |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 244.0±0.0 °C at 760 mmHg |
Melting Point | 38-40 °C(lit.) |
Molecular Formula | C9H8O |
Molecular Weight | 132.16 |
Flash Point | 111.7±0.0 °C |
Exact Mass | 132.057510 |
PSA | 17.07000 |
LogP | 2.10 |
Vapour Pressure | 0.0±0.4 mmHg at 25°C |
Index of Refraction | 1.585 |
Storage condition | -20°C |
Water Solubility | 6.5 g/L (20 C) |
1-Indanone, also known as indan-1-one or 1-indanone, is an organic compound with the chemical formula C9H8O. It is a cyclic ketone that consists of an indane ring system with a carbonyl group (C=O) attached to one of the carbon atoms.
Structure: 1-Indanone belongs to the class of compounds known as ketones, which are characterized by the presence of a carbonyl group (C=O) attached to two carbon atoms. It is derived from the fusion of a benzene ring and a cyclopentan ring, resulting in an indane structure. The carbonyl group is located on one of the sp2 hybridized carbon atoms of the indane ring.
Physical Properties: 1-Indanone is a white to off-white crystalline solid with a characteristic odor. It has a relatively high melting point and is sparingly soluble in water but soluble in organic solvents such as ethanol and aceton.
Uses and Applications: 1-Indanone is utilized as a building block or intermediate in the synthesis of various organic compounds. It serves as a precursor in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its reactivity as a ketone allows for various functional group transformations and reactions, making it useful in organic synthesis.
Chemical Reactions: Being a ketone, 1-indanone can undergo typical ketone reactions such as nucleophilic addition, reduction, and oxidation. It can also participate in condensation reactions and serve as a starting material for the synthesis of more complex molecules.
Biological Activities: Some derivatives of 1-indanone have shown interesting biological activities. For example, certain substituted 1-indanones have exhibited potential anticancer, antimicrobial, and anti-inflammatory properties. However, it should be noted that the biological activities can vary depending on the specific substitution pattern on the indanone core.
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