Identification | More | [Name]
4-Hydroxycyclohexanecarboxylic acid | [CAS]
17419-81-7 | [Synonyms]
4-HYDROXYCYCLOHEXANECARBOXYLIC ACID AKOS BB-9761 TIMTEC-BB SBB007787 4-Hydroxycyclohexylcarboxylic acid 4-HYDROXYCYCLOHEXANECARBOXYLIC ACID (CIS-AND TRANS-MIXTURE) 98+% 4-Hydroxycyclohexanecarboxylic Acid (cis-and trans-mixture) | [Molecular Formula]
C7H12O3 | [MDL Number]
MFCD00077974 | [Molecular Weight]
144.17 | [MOL File]
17419-81-7.mol |
Chemical Properties | Back Directory | [Melting point ]
120 °C | [Boiling point ]
307.9±35.0 °C(Predicted) | [density ]
1.246±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
almost transparency in Methanol | [form ]
powder to crystal | [pka]
4.72±0.10(Predicted) | [color ]
White to Almost white | [InChI]
InChI=1S/C7H12O3/c8-6-3-1-5(2-4-6)7(9)10/h5-6,8H,1-4H2,(H,9,10) | [InChIKey]
HCFRWBBJISAZNK-UHFFFAOYSA-N | [SMILES]
C1(C(O)=O)CCC(O)CC1 | [CAS DataBase Reference]
17419-81-7(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [HS Code ]
2918199890 |
Hazard Information | Back Directory | [Chemical Properties]
White crystal or colorless transparent viscous liquid | [Uses]
4-hydroxycyclohexanecarboxylic acid be used as organic intermediates. | [Definition]
ChEBI: 4-Hydroxycyclohexylcarboxylic acid is a hydroxy monocarboxylic acid. | [Synthesis]
The general procedure for the synthesis of cis-4-hydroxycyclohexanecarboxylic acid from methyl cis-4-hydroxycyclohexanecarboxylate was as follows: 20 g of methyl cis-4-hydroxycyclohexanecarboxylate was dissolved in 80 mL of methanol and cooled in an ice water bath. A 5 mol/L sodium hydroxide solution of 40 mL was slowly added, and after the drop was completed, the reaction mixture was stirred at room temperature overnight. After the reaction was completed, 150 mL of water was added to dilute it. The mixture was extracted twice with ethyl acetate and the organic phase was discarded. The aqueous phase was adjusted to pH 3 with 1 mol/L HCl and extracted twice with 50 mL of ethyl acetate to combine the organic phases. The organic phase was washed twice with saturated saline in turn, dried and decolorized. After filtration, the ethyl acetate was concentrated under reduced pressure to recover the ethyl acetate, and 16 g of white solid product was obtained in 90% yield. | [IC 50]
Human Endogenous Metabolite | [References]
[1] Patent: CN105061424, 2016, B. Location in patent: Paragraph 0029; 0031 |
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