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4-(4-FLUOROPHENOXY)BENZOIC ACID

CAS No.
129623-61-6
Chemical Name:
4-(4-FLUOROPHENOXY)BENZOIC ACID
Synonyms
4-(4-FLUOROPHENOXY)BENZOIC ACID;Benzoic acid, 4-(4-fluorophenoxy)-;4-(4-Fluorophenoxy)benzoic acid 97%;JR-7132, 4-(4-Fluorophenoxy)benzoic acid, 97%;4-(4-Fluorophenoxy)benzoic acid
CBNumber:
CB6705626
Molecular Formula:
C13H9FO3
Molecular Weight:
232.21
MDL Number:
MFCD01631892
MOL File:
129623-61-6.mol
MSDS File:
SDS
Last updated:2025-08-08 17:45:00

4-(4-FLUOROPHENOXY)BENZOIC ACID Properties

Melting point 171-175 °C
storage temp. Sealed in dry,Room Temperature
form solid
Appearance White to off-white Solid
UNSPSC Code 12352100

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H319-H400
Precautionary statements  P273-P301+P312+P330-P305+P351+P338
Hazard Codes  Xn,N
Risk Statements  22-36-50/53
Safety Statements  26-60-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3

4-(4-FLUOROPHENOXY)BENZOIC ACID price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 659487 4-(4-Fluorophenoxy)benzoic acid 97% 129623-61-6 1g $30 2023-06-20 Buy
Sigma-Aldrich 659487 4-(4-Fluorophenoxy)benzoic acid 97% 129623-61-6 5g $124 2023-06-20 Buy
TRC F621420 4-(4-Fluorophenoxy)benzoic acid 129623-61-6 250mg $55 2021-12-16 Buy
AK Scientific Z9479 4-(4-Fluorophenoxy)benzoic acid 129623-61-6 100g $611 2021-12-16 Buy
American Custom Chemicals Corporation COR0002666 4-(4-FLUOROPHENOXY)BENZOIC ACID 95.00% 129623-61-6 2.5G $852.21 2021-12-16 Buy
Product number Packaging Price Buy
659487 1g $30 Buy
659487 5g $124 Buy
F621420 250mg $55 Buy
Z9479 100g $611 Buy
COR0002666 2.5G $852.21 Buy

4-(4-FLUOROPHENOXY)BENZOIC ACID Chemical Properties,Uses,Production

Synthesis

4-Fluorobenzeneboronic acid

1765-93-1

Methylparaben

99-76-3

4-(4-FLUOROPHENOXY)BENZOIC ACID

129623-61-6

To a round bottom flask containing 4-fluorophenylboronic acid (2.1 g, 15 mmol), copper(II) acetate (1.4 g, 7.5 mmol), activated powdered molecular sieves (ca. 2 g), and nipagin methyl ester (1.2 g, 7.5 mmol) was added triethylamine (5.2 mL, 38 mmol) followed by dichloromethane (75 mL). The reaction mixture was stirred at room temperature for 16 hours while air was continuously passed through. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane and filtered through a silica gel column. The silica gel was washed with a solvent mixture of ethyl acetate-heptane. The filtrate was concentrated under reduced pressure and subsequently dissolved in 1,4-dioxane (15 mL). To this solution was added aqueous lithium hydroxide (1 N, 15 mL) and stirred at room temperature for 18 hours. At the end of the reaction, the pH of the reaction mixture was adjusted to acidic (pH < 6) with aqueous hydrochloric acid (1 N). The resulting precipitate was collected by filtration, washed with water and dried under vacuum to afford 4-(4-fluorophenoxy)benzoic acid (1.6 g, 90% yield). Mass spectrometry analysis (ESI) showed the (M-H)- peak of C13H9FO3 at m/z 231.

References

[1] Patent: US2003/236279, 2003, A1. Location in patent: Page 34

4-(4-FLUOROPHENOXY)BENZOIC ACID Preparation Products And Raw materials

4-(4-FLUOROPHENOXY)BENZOIC ACID Suppliers

Global( 63)Suppliers
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4-(4-FLUOROPHENOXY)BENZOIC ACID Spectrum

4-(4-FLUOROPHENOXY)BENZOIC ACID 4-(4-Fluorophenoxy)benzoic acid 97% Benzoic acid, 4-(4-fluorophenoxy)- JR-7132, 4-(4-Fluorophenoxy)benzoic acid, 97% 4-(4-Fluorophenoxy)benzoic acid 129623-61-6 FC6H4OC6H4CO2H C13H9FO3 Organic Building Blocks CARBOXYLIC ACID Building Blocks C13 to C42+ Carbonyl Compounds Carboxylic Acids C13 to C42+ Carbonyl Compounds Carboxylic Acids