ChemicalBook--->CAS DataBase List--->17419-81-7

17419-81-7

17419-81-7 Structure

17419-81-7 Structure
IdentificationMore
[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 PropertiesBack 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 DataBack 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 .
[WGK Germany ]

WGK 3
[HS Code ]

2918199890
[Storage Class]

12 - Non Combustible Liquids
[Hazard Classifications]

Eye Dam. 1
Hazard InformationBack 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]

Cyclohexanecarboxylic acid, 4-hydroxy-, Methyl ester, cis-

3618-03-9

cis-4-Hydroxycyclohexanecarboxylic acid

3685-22-1

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
Spectrum DetailBack Directory
[Spectrum Detail]

4-Hydroxycyclohexanecarboxylic acid(17419-81-7)MS
4-Hydroxycyclohexanecarboxylic acid(17419-81-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

4-Hydroxycyclohexanecarboxylic Acid  (cis-and trans-mixture),>98.0%(T)(17419-81-7)
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