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554332

Sigma-Aldrich

4-Fluorosalicylic acid

96%

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About This Item

Linear Formula:
FC6H3(OH)CO2H
CAS Number:
345-29-9
Molecular Weight:
156.11
EC Number:
206-459-5
MDL number:
MFCD00153168
UNSPSC Code:
12352100
PubChem Substance ID:
24879393
NACRES:
NA.22

Quality Level

100

Assay

96%

mp

170 °C (dec.) (lit.)

functional group

carboxylic acid
fluoro

SMILES string

OC(=O)c1ccc(F)cc1O

InChI

1S/C7H5FO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,(H,10,11)

InChI key

TTZOLDXHOCCNMF-UHFFFAOYSA-N

General description

4-Fluorosalicylic acid can be synthesized from the following compounds:
  • 4-fluorotoluene
  • m-fluorophenol
  • 4-aminosalicylic acid

Application

4-Fluorosalicylic acid may be used to synthesize 4-fluorogentisic acid.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

554332-1G:
554332-VAR:
554332-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBX2324V
MKBG6512V
MKBB5228
03218KD
05015HD

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Fluorosalicylohydroxamic acids.
Ostaszynski A, et al.
Bulletin de l'Academie Polonaise des Sciences. Serie des Sciences Chimiques, 8, 591-597 (1960)
Effect of intramolecular hydrogen bonding on the relative acidities of substituted salicylic acids in benzene solution.
Dunn GE and Penner TL.
Canadian Journal of Chemistry, 45(14), 1699-1706 (1967)
R L Crawford et al.
Journal of bacteriology, 121(3), 794-799 (1975-03-01)
Gentisate:oxygen 1,2-oxidoreductase (decyclizing) (EC 1.13.11.4; gentisate 1,2-dioxygenase) from Moraxella osloensis was purified to homogeneity as shown by polyacrylamide gel electrophoresis. The enzyme has a molecular weight of about 154,000 and gives rise to subunits of molecular weight 40,000 in the
Robin R Shields-Cutler et al.
The Journal of biological chemistry, 290(26), 15949-15960 (2015-04-12)
During Escherichia coli urinary tract infections, cells in the human urinary tract release the antimicrobial protein siderocalin (SCN; also known as lipocalin 2, neutrophil gelatinase-associated lipocalin/NGAL, or 24p3). SCN can interfere with E. coli iron acquisition by sequestering ferric iron

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