(2-((Perchlorophenoxy)carbonyl)-1H-indole-5-carbonyl)phosphonic acid CAS 2497586-25-9
| CAS No. | 2497586-25-9 |
| Molecular Formula | C16H7Cl5NO6P |
| Molecular Weight | 517.47 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.
CATO supplies (2-((Perchlorophenoxy)carbonyl)-1H-indole-5-carbonyl)phosphonic acid (CAS 2497586-25-9), a certified reference material (molecular formula C16H7Cl5NO6P, MW 517.47 g/mol) for analytical method development and quality control.
Structurally, (2-((Perchlorophenoxy)carbonyl)-1H-indole-5-carbonyl)phosphonic acid (C16H7Cl5NO6P) contains a flavonoid core, an amide group, a phosphate ester group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.5, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 517.47 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.
As a certified reference material (CRM), (2-((Perchlorophenoxy)carbonyl)-1H-indole-5-carbonyl)phosphonic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
Physical & Chemical Properties
| Molecular Formula | C16H7Cl5NO6P |
| Molecular Weight | 517.47 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor, low volatility) |
| Purity | 97%+ |
| Storage | Store at room temperature, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in methanol, acetonitrile, DMSO, water (slightly soluble) |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 11.5 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 2000 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 1 |
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