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CAS RN 530-78-9

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CAS RN 530-78-9

IUPAC Name: 2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid
Synonyms: flufenamic acid tecramine fluore-200 aluminum flufenamate fullsafe arlef acid, flufenamic reumajust A fluphenamic acid paraflu
Molecular Weight (g/mol): 281.23
Molecular Formula: C14H10F3NO2
InChi Key: LPEPZBJOKDYZAD-UHFFFAOYSA-N
SMILES: OC(=O)C1=CC=CC=C1NC1=CC=CC(=C1)C(F)(F)F
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Thermo Scientific Chemicals Flufenamic acid, 97%

CAS: 530-78-9 Molecular Formula: C14H10F3NO2 Molecular Weight (g/mol): 281.22 MDL Number: MFCD00002422 InChI Key: LPEPZBJOKDYZAD-UHFFFAOYSA-N Synonym: flufenamic acid,fluphenamic acid,nichisedan,achless,arlef,flufacid,fullsafe,lanceat,paraflu,plostene PubChem CID: 3371 ChEBI: CHEBI:42638 IUPAC Name: 2-[3-(trifluoromethyl)anilino]benzoic acid SMILES: C1=CC=C(C(=C1)C(=O)O)NC2=CC=CC(=C2)C(F)(F)F

PubChem CID 3371
CAS 530-78-9
Molecular Weight (g/mol) 281.22
ChEBI CHEBI:42638
MDL Number MFCD00002422
SMILES C1=CC=C(C(=C1)C(=O)O)NC2=CC=CC(=C2)C(F)(F)F
Synonym flufenamic acid,fluphenamic acid,nichisedan,achless,arlef,flufacid,fullsafe,lanceat,paraflu,plostene
IUPAC Name 2-[3-(trifluoromethyl)anilino]benzoic acid
InChI Key LPEPZBJOKDYZAD-UHFFFAOYSA-N
Molecular Formula C14H10F3NO2
2

Flufenamic Acid, Mikromol™

Discover Mikromol - your trusted source for high-quality pharmaceutical reference standards. Supporting accurate, compliant analysis with ISO 17034-accredited materials designed for confidence in every result.

3

Flufenamic Acid, LoGiCal

LoGiCal's certified reference materials as neats, native solutions and stable isotope labelled solutions, with expert documentation and support. From forensic to clinical labs, choose LoGiCal for confidence, compliance, and analytical excellence.

5

Flufenamic acid, MedChemExpress

MedChemExpress Flufenamic acid is a non-steroidal anti-inflammatory agent, inhibits cyclooxygenase (COX), activates AMPK, and also modulates ion channels, blocking chloride channels and L-type Ca2+ channels, modulating non-selective cation channels (NSC), activating K+ channels. Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes, such as cell migration and proliferation.

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