3-(4-Fluorophenyl)-N-(4-(pyridin-4-ylmethyl)phenyl)propanamide CAS 1377961-80-2
| CAS No. | 1377961-80-2 |
| Molecular Formula | C21H19FN2O |
| Molecular Weight | 334.39 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.
CATO supplies 3-(4-Fluorophenyl)-N-(4-(pyridin-4-ylmethyl)phenyl)propanamide (CAS 1377961-80-2), a certified reference material (molecular formula C21H19FN2O, MW 334.39 g/mol) for analytical method development and quality control.
Structurally, 3-(4-Fluorophenyl)-N-(4-(pyridin-4-ylmethyl)phenyl)propanamide (C21H19FN2O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 13.0, corresponding to approximately 13 ring(s) or double-bond equivalent(s). With a molecular weight of 334.39 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
CATO manufactures 3-(4-Fluorophenyl)-N-(4-(pyridin-4-ylmethyl)phenyl)propanamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.
Physical & Chemical Properties
| Molecular Formula | C21H19FN2O |
| Molecular Weight | 334.39 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 13.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1991 |
| Halogen Content | F-containing |
| Nitrogen Atoms | 2 |
Related Fluorophenyl Standards
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- Tris(4-fluorophenyl)phosphine (CAS 18437-78-0)
- Ethyl 2-((5-(4-fluorophenyl)-3,5-dihydro-1H-thieno[3,4-c]pyrrol-4-yl)amino)-2-oxoacetate (CAS 1172080-99-7)
- [4-(4-Fluorophenyl)-6-(1-methylethyl)-2-(methylsulfinyl)-5-pyrimidinyl]-ethyl Ester-d6 (CAS 1189487-47-5)
- 1-(2-Fluorophenyl)-3-((4-(thiophen-2-yl)tetrahydro-2H-pyran-4-yl)methyl)urea (CAS 1209628-84-1)
- Ethyl 4-((1-(3-fluorophenyl)-1H-tetrazol-5-yl)methyl)piperazine-1-carboxylate (CAS 1049407-95-5)
- 3-(4-Fluorophenyl)-6-(4-methoxyphenyl)pyrazolo[1,5-a]pyrimidin-7-amine (CAS 865657-97-2)
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Recommended Standards
- 3-(Cyclobutanecarboxamido)cyclohexyl (4-fluorophenyl)carbamate (CAS 1351616-03-9)
- tert-Butyl 7’-fluoro-2’-oxo-2’,4’-dihydro-1’H-spiro[piperidine-4,3’-quinoline]-1-carboxylate (CAS 1393330-69-2)
- Hydroxy Saxagliptin-13C3 (CAS 1346597-23-6)
- Tert-butyl 5'-fluoro-2'-oxo-1',4'-dihydro-2'H-spiro[piperidine-4,3'-quinoline]-1-carboxylate (CAS 1402232-78-3)
- 4-(1,3-Dioxaindan-5-yl)-3-(furan-2-yl)-1,2-oxazol-5-amine (CAS 1096939-74-0)
- 3-(4-Aminophenyl)-1H-pyridin-2-one (CAS 1352318-68-3)
- 2-Chloro-5-(tributylstannyl)pyrimidin-4-amine (CAS 597551-57-0)
- Methyl (2r,3s)-3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate (CAS 1176641-22-7)
- N-(Buta-1,3-dien-1-yl)benzothioamide (CAS 170937-98-1)
- 1-(Tert-butyl)azetidin-3-yl acetate (CAS 13619-16-4)
- 1-{1H-pyrrolo[2,3-b]pyridine-6-carbonyl}-4-(1,1,1-trifluoropropan-2-yl)piperazine (CAS 1947752-82-0)
- Benzyl N-(4-bromophenyl)-N-butylcarbamate (CAS 1881330-16-0)
- 2-[2-(4-methylphenoxy)ethoxy]ethan-1-ol (CAS 104-39-2)
- Peptide 438 (CAS CATO-CPTD788438)
Why CATO?
- ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
- 130,000+ catalog items in stock, COA supplied with every batch
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