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HCID 87364Erstellt: 26. Oktober 2026
2,5-Dimethoxybenzoylchlorid
BUTTPARK 48\04-28 · 2,5-DIMETHOXYBENZOYL CHLORIDE · Benzoyl chloride, 2,5-dimethoxy- · 2,5-Dimethoxybenzoic acid chloride · 2,5-DIMETHOXYBENZENE-1-CARBONYL CHLORIDE · carbamic acid [5-[(3-nitrophenyl)thio]-4-propan-2-yl-1-prop-2-enyl-2-imidazolyl]methyl ester
https://huagongshe.com/de/chemical/87364
Identifikatoren & physikalische Daten
| CAS No. | 17918-14-8 |
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| Summenformel | C9H9ClO3 |
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| Durchschnittliche Molmasse | 200,62 g/mol |
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| Monoisotopische Masse | 200,02402183 g/mol |
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| SMILES | COc1ccc(OC)c(C(=O)Cl)c1 |
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| InChIKey | YARKPRSRXZGKNI-UHFFFAOYSA-N |
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| PubChem CID | 87364 |
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| EC No. | 241-863-5 |
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| DTXSID | DTXSID00170777 |
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| Lokaler Name | 2,5-Dimethoxybenzoylchlorid |
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Chemische & physikalische Eigenschaften
| XLogP | 2,6 |
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| Polarare Oberfläche (TPSA) | 35,5 |
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| H-Brücken-Donoren | 0 |
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| H-Brücken-Akzeptoren | 3 |
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| Frei drehbare Bindungen | 3 |
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| Schwere Atome | 13 |
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| Formalladung | 0 |
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| Komplexität | 184 |
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| Schmelzpunkt | 53-54 °C(Solv: ligroine (8032-32-4)) |
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| Siedepunkt | 179°C/10mm |
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| Dichte | 1.224±0.06 g/cm3(Predicted) |
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| CAS Datenbank | 17918-14-8(CAS DataBase Reference) |
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Sicherheit & Vorschriften
| GHS-Einstufung | DangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
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| Hazard Classes and Categories | Skin Corr. 1B (100%) |
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| Zollcode | 2918999090 |
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Herstellung & Synthese
synthetische
AlCl3 (4.0 g, 30 mmol) was suspended in dichloromethane (30 mL). To this mixture, a solution of 1,4- dimethoxybenzene (1.38 g, 10 mmol) and triphosgene (5.94 g, 20 mmol) in dichloromethane (30 mL) was added dropwise over a period of 30 min. The resulting mixture was stirred under reflux for 7 days. It was then poured into crushed ice/ water (50 mL) and stirred with pyridine (0.5 mL) at 0 ℃ for 10 min. The layers were separated and the aqueous phase was extracted with dichloromethane (2 ×20 mL). The combined organic layers were washed with ice-cold 0.5 m HCl (30 mL) and with ice-cold water (2×10 mL), and dried over sodium sulfate. The solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel, eluting with hexane/ethyl acetate (4:1→3:1→2:1→1:1), to afford 1.23 g (60%) of 2,5-dimethoxybenzoyl chloride.