Name | 2-Chlorocyclohexanol |
Synonyms | Chlorocyclohexanol 2-Chlorocyclohexanol 2-CHLOROCYCLOHEXANOL Cyclohexanol, 2-chloro- 2-Chlorocyclohexane-1-ol CYCLOHEXENE CHLOROHYDRIN (1S,2R)-2-chlorocyclohexanol (1R,2R)-2-chlorocyclohexanol (1S,2S)-2-chlorocyclohexanol 2-CHLOROCYCLOHEXANOL, TECH., (1R,2S)-2-CHLORO-CYCLOHEXANOL (1R,2S)-2-chloro-1-cyclohexanol |
CAS | 1561-86-0 |
EINECS | 216-339-4 |
InChI | InChI=1/C6H11ClO/c7-5-3-1-2-4-6(5)8/h5-6,8H,1-4H2/t5-,6+/m0/s1 |
Molecular Formula | C6H11ClO |
Molar Mass | 134.6 |
Density | 1.13g/mLat 25°C(lit.) |
Melting Point | 29 °C |
Boling Point | 88-90°C 20mm |
Flash Point | 158°F |
Vapor Presure | 0.027mmHg at 25°C |
Appearance | Liquid |
Color | Clear colorless to light yellow |
pKa | 14.30±0.40(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.488(lit.) |
MDL | MFCD00003860 |
Physical and Chemical Properties | Colorless liquid. The relative density was 1.130, and the refractive index was nD20 1.4880. |
Use | For the synthesis of acaricide with low toxicity and high efficiency |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
HS Code | 29061900 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | organic synthesis intermediate. for the synthesis of low toxicity and high efficiency acaricide mites |
production method | cyclohexene and hypochlorous acid solution are vigorously stirred at 15-20 ℃ until the reaction solution is tested with potassium iodide and dilute hydrochloric acid. The color of iodine is not produced. Then add a second part of hypochlorous acid solution, repeat the reaction operation and test. When the reaction is completed, the reactants settle out of the oil layer, and a little excess hypochlorous acid should be present in the test with potassium iodide. The resulting 2-chlorocyclohexanol can be separated by distillation. |