Name | 2-Indanone |
Synonyms | 2-Indanon 2-INDANONE 2-Indanone Indan-2-one INDANONE(2-) 2-Hydrindone 2-Oxohydrindene 1,3-dihydro-2h-inden-2-on 1,3-Dihydro-2H-inden-2-one 1,3-dihydro-2H-inden-2-one 2H-Inden-2-one,1,3-dihydro- 1,3-dihydro-,2H-inden-2-one |
CAS | 615-13-4 |
EINECS | 210-410-3 |
InChI | InChI=1/C9H8O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4H,5-6H2 |
InChIKey | UMJJFEIKYGFCAT-UHFFFAOYSA-N |
Molecular Formula | C9H8O |
Molar Mass | 132.16 |
Density | 1.0712 |
Melting Point | 51-54 °C (lit.) |
Boling Point | 218°C |
Flash Point | 212°F |
Water Solubility | insoluble |
Solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) |
Vapor Presure | 0.0236mmHg at 25°C |
Appearance | Crystallization |
Color | Light yellow to yellow-brown |
BRN | 636550 |
Storage Condition | 2-8°C |
Sensitive | Hygroscopic |
Refractive Index | 1.5380 (estimate) |
MDL | MFCD00003792 |
Physical and Chemical Properties | Needle-like crystals (ethanol or ether), volatile with water vapor, melting point 58-61 °c, flash point 100 °c. |
Use | An intermediate of ambolidine (indenylamine). |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
RTECS | NK7535500 |
FLUKA BRAND F CODES | 3 |
TSCA | Yes |
HS Code | 29145090 |
Hazard Note | Irritant |
olfactory Threshold | 0.00036ppm |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | an intermediate of ambolidine (indenylamine). An intermediate of ambolidine (indenylamine); Used in the preparation of drugs such as apentin and cefalet. |
production method | 1. Preparation Method: indan-1, 2-diol monoformate (3): add 88% formic acid to the reaction bottle equipped with stirrer, thermometer and dropping funnel (), 30% mL(1.37mol) of hydrogen peroxide, indene (2)116.2g[117.3mL,1.0mol(98%)] was slowly added dropwise under stirring at 35-40 ° C. For about 2 hours. Finally 100ml of formic acid was added to rinse the dropping funnel. The reaction was stirred at room temperature for 7H to complete the reaction. Formic acid (2.66-4.0kPa) was distilled off under reduced pressure and the residue was cooled to room temperature to give a light brown solid (3). 2-indanone (1): 7% of sulfuric acid 2L and compound (3) were added to a distillation flask, and steam distillation was performed. The outflow rate is about 1L/h, and the volume of the reaction bottle is kept at about 2L by adding water at any time. A total of 5-6L of distillate is collected. The dark brown liquid in the bottle became semi-solid after cooling. The distillate was cooled and filtered to obtain a white solid. After drying under vacuum for more than 12h, 90 ~ 107g of compound (1) was obtained, mp57 ~ 58 ℃, yield 69% ~ 81%. [1] |