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Cyclohexylacetic acid

Cyclohexylacetic acid

CAS: 5292-21-7

Molecular Formula: C8H14O2

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Cyclohexylacetic acid - Names and Identifiers

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)

Cyclohexylacetic acid - Physico-chemical Properties

Molecular FormulaC8H14O2
Molar Mass142.2
Density1.007 g/mL at 25 °C(lit.)
Melting Point29-31°C(lit.)
Boling Point242-244°C(lit.)
Flash Point>230°F
JECFA Number965
Vapor Presure0.00961mmHg at 25°C
AppearanceLow Melting Solid
ColorWhite to pale yellow
BRN2041326
pKapK1:4.51 (25°C)
Storage ConditionSealed in dry,Room Temperature
Refractive Indexn20/D 1.463(lit.)
MDLMFCD00001518

Cyclohexylacetic acid - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR37/38 - Irritating to respiratory system and skin.
R41 - Risk of serious damage to eyes
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
WGK Germany3
RTECSGU8370000
TSCAYes
HS Code29162090
Hazard NoteIrritant

Cyclohexylacetic acid - Reference Information

FEMA2347 | 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]
Last Update:2024-04-09 21:54:55
Cyclohexylacetic acid
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View History
Cyclohexylacetic acid
bromochloro-methane
Cinchonidine
3-Amino-2-phenylimidazo(1,2-a)pyridine
Formic acid, azodi-, diethyl ester
Ethanol, 2-ethoxy-
339-17-3
DIPHENYLTHIOMETHANE
1-amino-2-[2-(2-methoxyethoxy)ethoxy]-4-(2,4,6-trimethylanilino)anthracene-9,10-dione
methylbensulfuron
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