6-Fluorochromane-2-carboxylic acid

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Products Intro: Product Name:6-Fluorochromane-2-carboxylic acid
CAS:99199-60-7
Purity:0.99 Package:1kg Remarks:MG25988
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Products Intro: Product Name:6-Fluorochromane-2-carboxylic acid
CAS:99199-60-7
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Products Intro: Product Name:6-Fluorochromane-2-carboxylic acid
CAS:99199-60-7
Purity:98% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:6-fluorochromane-2-carboxylic acid
CAS:99199-60-7
Purity:99% Package:25KG;5KG;1KG
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Products Intro: CAS:99199-60-7
Purity:98% Package:g-Kg Remarks:White to white powder

6-Fluorochromane-2-carboxylic acid manufacturers

6-Fluorochromane-2-carboxylic acid Basic information
Product Name:6-Fluorochromane-2-carboxylic acid
Synonyms:6-FLUOROCHROMANE-2-CARBOXYLIC ACID;rac-6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic Acid;6-Fluoro-3,4-dihydro-2H-benzopyran-2-carboxylic acid;6-Fluorochromane-2-carboxylic acid (FCC III);6-Fluorochromane-2-carboxylicaci;6-Fluoro-3,4-dihydro-2H- 1-benzopryan-2-carboxylic acid;6-Fluoro -3,4-Dihydro2h -1-Benzopyran - Benzoyl 2-Carboxylic Acid (NB -3);2H-1-BENZOPYRAN-2-CARBOXYLIC ACID, 6-FLUORO-3,4-DIHYDRO-
CAS:99199-60-7
MF:C10H9FO3
MW:196.18
EINECS:619-405-4
Product Categories:Heterocycles;Intermediates;Carboxylic Acids;Carboxylic Acids;Intermediates & Fine Chemicals;Pharmaceuticals;Fused Ring Systems
Mol File:99199-60-7.mol
6-Fluorochromane-2-carboxylic acid Structure
6-Fluorochromane-2-carboxylic acid Chemical Properties
Melting point 129.2-130.3 ºC
Boiling point 358.0±42.0 °C(Predicted)
density 1.364±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka3.05±0.20(Predicted)
color White to Off-White
InChIInChI=1S/C10H9FO3/c11-7-2-4-8-6(5-7)1-3-9(14-8)10(12)13/h2,4-5,9H,1,3H2,(H,12,13)
InChIKeyZNJANLXCXMVFFI-UHFFFAOYSA-N
SMILESC1(C(O)=O)OC2=CC=C(F)C=C2CC1
Safety Information
HS Code 2932990090
MSDS Information
6-Fluorochromane-2-carboxylic acid Usage And Synthesis
Chemical PropertiesOff-White Solid
UsesNebivolol intermediate.
Synthesis
6-Fluorochromone-2-carboxylic acid

99199-59-4

6-Fluorochromane-2-carboxylic acid

99199-60-7

General procedure for the synthesis of 6-fluorobenzodihydropyran-2-carboxylic acid from 6-fluoro-4-oxo-4H-1-benzopyran-2-carboxylic acid: 30 g (0.144 mol) of 6-fluoro-4-oxo-4H-1-benzopyran-2-carboxylic acid, 5 g of wet palladium-carbon (5% Pd/carbon, 50% aqueous content) and 500 mL of glacial acetic acid were placed in an autoclave. After sealing three times under nitrogen protection, the nitrogen was replaced with hydrogen. Subsequently, the hydrogen was pressurized to 2.0 MPa and the reactor was heated to 7080°C. During the reaction, when the hydrogen pressure in the kettle dropped, the hydrogen was promptly replenished to 2.0 MPa. The reaction was considered to be completed when the reactor pressure remained stable and did not change any more within half an hour. After the reaction was completed, the hydrogen in the autoclave was released and the reaction solution was filtered to recover the Pd/C catalyst. The filtrate was concentrated under reduced pressure to recover glacial acetic acid. The remaining concentrate was poured into 30 mL of petroleum ether and heated to give a white crystalline solid. The solid was filtered and dried to give a final 25 g of white 6-fluorobenzodihydropyran-2-carboxylic acid solid in 88.4% yield and 99.8% purity.

References[1] Patent: CN104072470, 2016, B. Location in patent: Paragraph 0060; 0061
[2] Journal of Chemical Research, 2006, # 12, p. 807 - 808
[3] Patent: US6545040, 2003, B1
[4] Patent: US4654362, 1987, A
[5] Patent: US2004/82592, 2004, A1
6-Fluorochromane-2-carboxylic acid Preparation Products And Raw materials
Raw materials6-Fluorochromone-2-carboxylic acid
Preparation Products2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanone
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