Grundinformationen
- Standard-SMILES
COc1ccc(OC)c(C(=O)Cl)c1- InChIKey
YARKPRSRXZGKNI-UHFFFAOYSA-N- Summenformel
- C9H9ClO3
- Durchschnittliche Molmasse
- 200,62 g/mol
- Monoisotopische Masse
- 200,02402183
Namen und Bezeichner
- Bevorzugter Name
- 2,5-Dimethoxybenzoyl chloride
- IUPAC
- 2,5-dimethoxybenzoyl chloride
- Lokaler Name
- 2,5-Dimethoxybenzoylchlorid
- Englischer Name
- 2,5-DIMETHOXYBENZOYL CHLORIDE
- Summenformel
- C9H9ClO3
- Molmasse
- 200.62
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
17918-14-8- PubChem CID
- 87364
- DTXSID
DTXSID00170777- EC Number
- 241-863-5
- Nikkaji
- J260.796D
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 2,6
- Polarare Oberfläche (TPSA)
- 35,5 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 13
- Formalladung
- 0
- Komplexität
- 184
Physikochemische Eigenschaften
- Schmelzpunkt
- 53 · 53-54 °C(Solv: ligroine (8032-32-4))
- Siedepunkt
- 179 °C/10mm · 179°C/10mm
- Dichte
- 1.224 · 1.224±0.06 g/cm3(Predicted)
- CAS Datenbank
- 17918 · 17918-14-8(CAS DataBase Reference)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H314 (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.
Gefahrenhinweise
Sicherheitsdaten
- hs_code
- 2918999090
Chemie und Industrie
Darstellung
synthetischeAlCl3 (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.
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