Name | 1,4-Cyclohexanedione |
Synonyms | Tetrahydroquinone 1,4-Cyclohexandion 1,4-CYCHEXANEDIONE 1,4-CYCLOHEXANDIONE Cyclohexan-1,4-dione 1,4-Dioxocyclohexane 1,4-Cyclohexanedione 1,4-Cyclohexane Dione cyclohexane-1,4-dione tetrahydro-p-benzoquinone TETRAHYDRO-P-BENZOQUINONE |
CAS | 637-88-7 |
EINECS | 211-306-0 |
InChI | InChI=1/C6H8O2/c7-5-1-2-6(8)4-3-5/h1-4H2 |
Molecular Formula | C6H8O2 |
Molar Mass | 112.13 |
Density | 1.0861 |
Melting Point | 77-78.5 °C (lit.) |
Boling Point | 112 °C (19.5026 mmHg) |
Flash Point | 132 °C |
Solubility | Soluble in methanol and ethanol. |
Vapor Presure | 0.0809mmHg at 25°C |
Appearance | Crystallization |
Color | Light yellow to yellow or beige |
BRN | 774152 |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Stability | Stable. Combustible. Incompatible with strong oxidizing agents. |
Refractive Index | 1.4570 (estimate) |
MDL | MFCD00001606 |
Physical and Chemical Properties | Melting point 76-80°C boiling point 112°C (19.5026 mmHg) flash point 132°C |
Use | For pharmaceutical, synthetic electrical conductor materials |
Hazard Symbols | Xi - Irritant |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
FLUKA BRAND F CODES | 8 |
TSCA | Yes |
HS Code | 29142900 |
Hazard Note | Irritant |
colorless crystals. Soluble in chloroform, ethanol, insoluble in petroleum ether, ether.
add the prepared sodium ethoxide to the reaction kettle, add diethyl ether and diethyl succinate, dissolve in water and reflux for 3 days, recover the diethyl ether; Then cool to room temperature, add 10% dilute sulfuric acid to adjust to pH = 2, the crystals were filtered off, washed with water, and dried to give crude diethyl succinate; The crude product was recrystallized from ethanol (melting point 127-129 ° C.) to give a pure product. Then add diethyl succinate back to the flask, add the mixture of concentrated sulfuric acid, water and ethanol, refluxed in oil for 5 days, cool, neutralize with ammonia water to pH = 8, and then extract 4 times with chloroform, the crude product is obtained by recovering chloroform; The crude product is then subjected to vacuum distillation, and the distillate is poured into cold petroleum ether, filtered and dried, I .e., 1,4-cyclohexanedione product.
This product is used in organic synthesis and is also a general reagent.
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | used in pharmaceutical, synthetic electrical conductor materials, This product is used in organic synthesis, medicine, synthesis of electrical conductor materials, etc. It is also a universal reagent. Medicine, liquid crystal intermediate, used in the synthesis of conductivity. |
production method | Add prepared sodium ethoxide into the reaction kettle, then add diethyl ether and diethyl succinate, dissolve in water and reflux for 3 days, recovering diethyl ether; Then cooling to room temperature, adding 10% dilute sulfuric acid to adjust to pH = 2, filtering out the crystals, washing with water, and drying to obtain crude diethyl succinate; the crude product was recrystallized from ethanol (melting point 127-129 °c) to obtain a pure product. Then add diethyl succinate back to the flask, add the mixture of concentrated sulfuric acid, water and ethanol, refluxed in oil for 5 days, cool, neutralize with ammonia water to pH = 8, and then extract 4 times with chloroform, the chloroform was recovered to obtain a crude product; The crude product was then subjected to distillation under reduced pressure, and the distillate was poured into cold petroleum ether, filtered, and air-dried, I .e., 1, 4-cyclohexanedione product. |