Name | Cyclohexylacetic acid |
Synonyms | NCI 204816 AKOS BBS-00003723 2-cyclohexylacetate Cyclohexylacetic acid Cycloxhexylacetic acid Cyclohexaneacetic acid 2-Cyclohexylacetic acid 2-Cyclohexylethanoic acid, (Carboxymethyl)cyclohexane |
CAS | 5292-21-7 |
EINECS | 226-132-0 |
InChI | InChI=1/C8H14O2/c9-8(10)6-7-4-2-1-3-5-7/h7H,1-6H2,(H,9,10) |
Molecular Formula | C8H14O2 |
Molar Mass | 142.2 |
Density | 1.007 g/mL at 25 °C(lit.) |
Melting Point | 29-31°C(lit.) |
Boling Point | 242-244°C(lit.) |
Flash Point | >230°F |
JECFA Number | 965 |
Vapor Presure | 0.00961mmHg at 25°C |
Appearance | Low Melting Solid |
Color | White to pale yellow |
BRN | 2041326 |
pKa | pK1:4.51 (25°C) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.463(lit.) |
MDL | MFCD00001518 |
Hazard Symbols | Xi - Irritant![]() |
Risk Codes | R37/38 - Irritating to respiratory system and skin. R41 - Risk of serious damage to eyes R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | 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 |
RTECS | GU8370000 |
TSCA | Yes |
HS Code | 29162090 |
Hazard Note | Irritant |
FEMA | 2347 | CYCLOHEXANEACETIC ACID |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
biological activity | Cyclohexaneacetic acid is a perfume ingredient. |
production method | 1. preparation method: add palladium acetate 4.5mg(0.02mmol),1,4-bis (diphenylphosphine) butane (dppb)17mg(0.04mmol),5.0mmol formic acid and 5mL dimethoxyethane into a pressure reactor. Methylene cyclohexane (2)24mg,(2.5mmol) is added, and carbon monoxide gas is introduced until the pressure reaches 0.68Mpa. Heat to 150 ℃ and stir for 16h. Cold to room temperature, open the reactor. The solvent is evaporated under reduced pressure, and sodium hydroxide solution is added to the residue to dissolve it. Ether extraction, water layer acidified with hydrochloric acid. Ether extraction 3 times, combined with ether layer, anhydrous sodium sulfate drying. Concentrate to obtain compound (1) with 94% yield. The following compounds can be synthesized by similar synthesis methods (table I-8-5, reference book 422 pages). [1] |