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5-Fluorosalicylic acid - >98.0%, high purity , CAS No.345-16-4

    Grade & Purity:
  • ≥98%
In stock
Item Number
F113843
Grouped product items
SKU Size
Availability
Price Qty
F113843-250mg
250mg
3
$9.90
F113843-1g
1g
10
$10.90
F113843-5g
5g
3
$19.90
F113843-25g
25g
4
$69.90
F113843-100g
100g
1
$229.90

Basic Description

Synonyms A18672 | BDBM50219484 | F0469 | EINECS 206-455-3 | NSC-46619 | PS-8850 | AM20040223 | DTXSID00188054 | JWPRICQKUNODPZ-UHFFFAOYSA-N | CK2251 | EN300-49122 | NSC 46619 | 5-Fluoro-2-hydroxybenzoicacid | SCHEMBL130520 | 2-Hydroxy-5-fluorobenzoic acid | 2-hydr
Specifications & Purity ≥98%
Storage Temp Room temperature
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Benzoic acids and derivatives
Intermediate Tree Nodes Hydroxybenzoic acid derivatives - Salicylic acid and derivatives
Direct Parent Salicylic acids
Alternative Parents Halobenzoic acids  3-halobenzoic acids  Benzoic acids  P-fluorophenols  Benzoyl derivatives  Fluorobenzenes  1-hydroxy-2-unsubstituted benzenoids  Aryl fluorides  Vinylogous acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organooxygen compounds  Organofluorides  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Halobenzoic acid - 3-halobenzoic acid - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Salicylic acid - Benzoic acid - 4-fluorophenol - Benzoyl - 4-halophenol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Vinylogous acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Organooxygen compound - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Organic oxide - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as salicylic acids. These are ortho-hydroxylated benzoic acids.
External Descriptors Not available

Associated Targets(Human)

ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MMP3 Tchem Matrix metalloproteinase 3 (3433 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MMP8 Tchem Matrix metalloproteinase 8 (1942 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MMP1 Tchem Matrix metalloproteinase-1 (7046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DAO Tchem D-amino-acid oxidase (802 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp2 Matrix metalloproteinase-2 (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAW264.7 (28094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488183977
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183977
IUPAC Name 5-fluoro-2-hydroxybenzoic acid
INCHI InChI=1S/C7H5FO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)
InChIKey JWPRICQKUNODPZ-UHFFFAOYSA-N
Smiles C1=CC(=C(C=C1F)C(=O)O)O
Isomeric SMILES C1=CC(=C(C=C1F)C(=O)O)O
WGK Germany 3
Molecular Weight 156.11
Beilstein 2209120
Reaxy-Rn 2209120
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2209120&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number Certificate Type Date Item
E1723015 Certificate of Analysis Jan 20, 2025 F113843
C2511206 Certificate of Analysis Jun 25, 2024 F113843
C2511380 Certificate of Analysis Jun 25, 2024 F113843
F2008082 Certificate of Analysis Mar 05, 2024 F113843
G2313121 Certificate of Analysis Jul 21, 2023 F113843
D2312272 Certificate of Analysis Sep 19, 2021 F113843
G2313114 Certificate of Analysis Sep 19, 2021 F113843
G2313112 Certificate of Analysis Sep 19, 2021 F113843

Chemical and Physical Properties

Solubility Slightly soluble in water.
Melt Point(°C) 180°C
Molecular Weight 156.110 g/mol
XLogP3 2.600
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 1
Exact Mass 156.022 Da
Monoisotopic Mass 156.022 Da
Topological Polar Surface Area 57.500 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 160.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yanwen Guo, Zhenzhen Cai, Fei Yan, Da Lei, Yanan Guo, Shuhai Zhang, Xincun Dou.  (2023)  Precise Electron-Withdrawing Strength Modulation of ESIPT Probes for Ultrasensitive and Specific Fluorescence Sensing.  ANALYTICAL CHEMISTRY,  95  (23): (9014–9024). 
2. Mei-Yan Gao, Kai Wang, Yayong Sun, Dejing Li, Bai-Qiao Song, Yassin H. Andaloussi, Michael J. Zaworotko, Jian Zhang, Lei Zhang.  (2020)  Tetrahedral Geometry Induction of Stable Ag–Ti Nanoclusters by Flexible Trifurcate TiL3 Metalloligand.  Journal of the American Chemical Society,  142  (29): (12784–12790). 
3. Bang-Chang Zhu, Wei-Hui Fang, Perumal Emayavaramban, Lei Zhang, Jian Zhang.  (2018)  Structures and photophysical performances of (fluoro)salicylate stabilized polyoxo-titanium clusters.  CRYSTENGCOMM,  20  (39): (5964-5968). 

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