Name | 3-Coumaranone |
Synonyms | 3-Coumaranone 3-Oxocoumaran Benzofuran-3-one benzofuran-3(2H)-one 1-benzofuran-3(2H)-one 1-Benzofuran-3(2H)-one Benzo[b]furan-3(2H)-one 2,3-dihydro-1-benzofuran-2-one 3-Coumaranonebenzofuran-3(2H)-one 1-Benzofuran-3(2H)-one, Coumaran-3-one 1-Benzofuran-3(2H)-one, Coumaran-3-one, 2,3-Dihydro-3-oxo-1-benzofuran |
CAS | 7169-34-8 |
EINECS | 640-279-1 |
InChI | InChI=1/C8H6O2/c9-7-5-10-8-4-2-1-3-6(7)8/h1-4H,5H2 |
Molecular Formula | C8H6O2 |
Molar Mass | 134.13 |
Density | 1.1603 (rough estimate) |
Melting Point | 101-103 °C |
Boling Point | 207.23°C (rough estimate) |
Flash Point | 118.944°C |
Water Solubility | Slightly miscible with water. |
Solubility | Chloroform (Slightly), DMSO (Slightly) |
Vapor Presure | 0.023mmHg at 25°C |
Appearance | Crystallization |
Color | Yellow to Dark Yellow |
BRN | 115296 |
Storage Condition | Keep in dark place,Sealed in dry,Store in freezer, under -20°C |
Sensitive | Light Sensitive |
Refractive Index | 1.4800 (estimate) |
MDL | MFCD00051810 |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 4.5-9 |
HS Code | 29329990 |
Hazard Note | Irritant |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
Introduction | , 3-benzofuran ketone compounds have good physiological activity, and its derivatives have antibacterial, antiviral, antioxidant and other effects.|
Application | 3-benzofuran ketones are also important pharmaceutical and chemical intermediates, which can be widely used in the synthesis of pharmaceuticals, pesticides, new antioxidants and food additives. For this reason, it is of great practical significance and application value to develop a practical and efficient method for the synthesis of 3-benzofuranones. |
preparation | under normal temperature and pressure, dissolve 0.2mmol of 2-ethynylphenol in 1ml of dichloromethane, to a solution of 2-ethynylphenol in methylene chloride, 0.01mmol of Mercury triflate and 0.24mmol of pyridine-N-oxide were added, the mixture was stirred at room temperature for 1 hour at a stirring rate of 600r/min, and 3-benzofuranone was reacted to form. 24.7mg of 3-benzofuranone was obtained by silica gel column chromatography, and the yield was 92.2%. |