6-Hydroxyindan-1-one
6-Hydroxy-1-Indenone
CAS: 62803-47-8
Molecular Formula: C9H8O2
6-Hydroxyindan-1-one - Names and Identifiers
| Name | 6-Hydroxy-1-Indenone |
| Synonyms | 6-Hydroxyindan-1-one 6-Hydroxy-1-Indenone 6-Hydroxy-1-Indanone 6-Hydroxy-1-indanone 6-HYDROXY-1-INDANONE 6-hydroxy-2,3-dihydroinden-1-one 6-Hydrocy-2,3-Dihydro-1H-Inden-1-One 2,3-Dihydro-6-hydroxy-1H-inden-1-one 6-Hydroxy-2,3-dihydro-1H-inden-1-one 6-hydroxy-2,3-dihydro-1H-inden-1-one |
| CAS | 62803-47-8 |
| InChI | InChI=1/C9H8O2/c10-7-3-1-6-2-4-9(11)8(6)5-7/h1,3,5,10H,2,4H2 |
| InChIKey | MOANRQDXNNXOLW-UHFFFAOYSA-N |
6-Hydroxyindan-1-one - Physico-chemical Properties
| Molecular Formula | C9H8O2 |
| Molar Mass | 148.16 |
| Density | 1.305±0.06 g/cm3(Predicted) |
| Melting Point | 154-158 °C (lit.) |
| Boling Point | 329.0±31.0 °C(Predicted) |
| Flash Point | 139.8°C |
| Vapor Presure | 9.51E-05mmHg at 25°C |
| pKa | 9.45±0.20(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.631 |
| MDL | MFCD00513530 |
| Physical and Chemical Properties | Appearance: light yellow to white crystal Melting Point: 155-158 ℃ |
6-Hydroxyindan-1-one - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R36/38 - Irritating to eyes and skin. R43 - May cause sensitization by skin contact |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
| WGK Germany | 2 |
| HS Code | 29145090 |
6-Hydroxyindan-1-one - Introduction
6-Hydroxy-1-Indenone(6-Hydroxy-1-Indenone) is an organic compound with the chemical formula C9H6O2 and a molecular weight of 146.14.
Nature:
6-Hydroxy-1-Indenone is a light yellow crystalline solid. It has a hydroxyl group and a ketone group fixed at the 1 and 6 positions of the indene ring. It is soluble in alcohol, ether and chloroform and insoluble in water.
Use:
6-Hydroxy-1-Indenone has certain chemical reactivity and is often used as an intermediate in organic synthesis. It can participate in the construction of C- C bonds, the synthesis of heterocyclic reactions. It can also be used as a synthetic raw material for dyes and pigments, for the preparation of organic photosensitive materials, and for the synthesis of some drugs.
Preparation Method:
A common method for preparing 6-Hydroxy-1-Indenone is through the hydrogen oxidation reaction of the indene ring. A common synthetic method is to react an indanone with an oxidizing agent (such as chromic acid) under acidic conditions to give 6-Hydroxy-1-Indenone by oxidizing the carbonyl group on the indene ring.
Safety Information:
There are no detailed reports on the safety of 6-Hydroxy-1-Indenone. However, as a general rule for handling organic compounds, operations should follow appropriate laboratory safety operations, including wearing personal protective equipment (such as safety glasses, gloves and laboratory coats) and operations in a well-ventilated area. It is also necessary to properly store, treat and dispose of waste and to avoid undue contact with other chemicals. Before use, it is recommended to carefully read and follow the chemical safety instructions provided by the supplier. If you have any questions or need more detailed information, please consult a professional chemist or institution.
Nature:
6-Hydroxy-1-Indenone is a light yellow crystalline solid. It has a hydroxyl group and a ketone group fixed at the 1 and 6 positions of the indene ring. It is soluble in alcohol, ether and chloroform and insoluble in water.
Use:
6-Hydroxy-1-Indenone has certain chemical reactivity and is often used as an intermediate in organic synthesis. It can participate in the construction of C- C bonds, the synthesis of heterocyclic reactions. It can also be used as a synthetic raw material for dyes and pigments, for the preparation of organic photosensitive materials, and for the synthesis of some drugs.
Preparation Method:
A common method for preparing 6-Hydroxy-1-Indenone is through the hydrogen oxidation reaction of the indene ring. A common synthetic method is to react an indanone with an oxidizing agent (such as chromic acid) under acidic conditions to give 6-Hydroxy-1-Indenone by oxidizing the carbonyl group on the indene ring.
Safety Information:
There are no detailed reports on the safety of 6-Hydroxy-1-Indenone. However, as a general rule for handling organic compounds, operations should follow appropriate laboratory safety operations, including wearing personal protective equipment (such as safety glasses, gloves and laboratory coats) and operations in a well-ventilated area. It is also necessary to properly store, treat and dispose of waste and to avoid undue contact with other chemicals. Before use, it is recommended to carefully read and follow the chemical safety instructions provided by the supplier. If you have any questions or need more detailed information, please consult a professional chemist or institution.
Last Update：2024-04-09 21:54:55
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Product Name: 6-Hydroxy-1-indanone Visit Supplier Webpage Request for quotationCAS: 62803-47-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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