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4,4-Difluorocyclohexanecarboxylic acid

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CAS:122665-97-8
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CAS:122665-97-8
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CAS:122665-97-8
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4,4-Difluorocyclohexanecarboxylic acid manufacturers

4,4-Difluorocyclohexanecarboxylic acid Basic information
Product Name:4,4-Difluorocyclohexanecarboxylic acid
Synonyms:4,4-DIFLUOROCYCLOHEXANECARBOXYLIC ACID;Cyclohexanecarboxylic acid, 4,4-difluoro-;4,4-DIFLUOROCYCLOHEXYLCARBOXYLIC ACID;Maraviroc Intermediate 1;4,4-diflurocyclohexane carboxylic acid;4,4 - Difluorocyclohexanecarboxylicd;4,4-difluorocyclohexane-1-carboxylic acid;4,4-Difluorocyclohexanecarboxylic acid(HXFA)
CAS:122665-97-8
MF:C7H10F2O2
MW:164.15
EINECS:602-802-1
Product Categories:Intermediates & Fine Chemicals;Pharmaceuticals;Drug Intermediates;Carboxylic Acids;Ring Systems;C7;Carbonyl Compounds;Aliphatics
Mol File:122665-97-8.mol
4,4-Difluorocyclohexanecarboxylic acid Structure
4,4-Difluorocyclohexanecarboxylic acid Chemical Properties
Melting point 103-107 °C
Boiling point 241.1±40.0 °C(Predicted)
density 1.24±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Methanol
form Solid
pka4.06±0.10(Predicted)
color White
InChIInChI=1S/C7H10F2O2/c8-7(9)3-1-5(2-4-7)6(10)11/h5H,1-4H2,(H,10,11)
InChIKeyHYIUDFLDFSIXTR-UHFFFAOYSA-N
SMILESC1(C(O)=O)CCC(F)(F)CC1
CAS DataBase Reference122665-97-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
HazardClass IRRITANT
HS Code 29161900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
4,4-Difluorocyclohexanecarboxylic acid Usage And Synthesis
Chemical Properties4,4-Difluorocyclohexanecarboxylic acid is White Solid
Uses4,4-Difluorocyclohexanecarboxylic acid is a di-substituted cyclohexane carboxylic acids used in the synthesis of macrolide antibiotics.
Synthesis
ETHYL 4,4-DIFLUOROCYCLOHEXANECARBOXYLATE

178312-47-5

4,4-Difluorocyclohexanecarboxylic acid

122665-97-8

The general procedure for the synthesis of 4,4-difluorocyclohexanecarboxylic acid from ethyl 4,4-difluorocyclohexanecarboxylate was as follows: ethyl 4,4-difluorocyclohexanecarboxylate (0.385 g, 2.003 mmol) was dissolved in THF (12 mL), and H2O (6 mL) was added, followed by lithium hydroxide monohydrate (0.420 g, 10.02 mmol). The reaction mixture was stirred vigorously at room temperature overnight. Upon completion of the reaction, the mixture was diluted with EtOAc and the pH was adjusted to 4 with 1 M HCl. The organic and aqueous layers were separated, and the aqueous layer was then extracted with EtOAc (1 time). The organic phases were combined, washed with brine, dried over MgSO4 and concentrated to dryness to give 4,4-difluorocyclohexanecarboxylic acid (318 mg, 97% yield) as a white solid.1H NMR (400 MHz, DMSO-d6): δ 12.28 (s, 1H), 2.40 (m, 1H), 2.02-1.75 (m, 6H), 1.59 (m, 2H) .

References[1] Patent: US2014/275080, 2014, A1. Location in patent: Paragraph 0428
[2] Patent: WO2013/13188, 2013, A1. Location in patent: Paragraph 00313; 00314
[3] Patent: US9416132, 2016, B2. Location in patent: Page/Page column 134; 135
[4] Organic Letters, 2018, vol. 20, # 16, p. 4959 - 4963
[5] Patent: US2008/146605, 2008, A1. Location in patent: Page/Page column 39-40
Tag:4,4-Difluorocyclohexanecarboxylic acid(122665-97-8) Related Product Information
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