Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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

Molekülstruktur von 2,5-Dimethoxybenzoylchlorid

Identifikatoren & physikalische Daten

CAS No.17918-14-8
SummenformelC9H9ClO3
Durchschnittliche Molmasse200,62 g/mol
Monoisotopische Masse200,02402183 g/mol
SMILESCOc1ccc(OC)c(C(=O)Cl)c1
InChIKeyYARKPRSRXZGKNI-UHFFFAOYSA-N
PubChem CID87364
EC No.241-863-5
DTXSIDDTXSID00170777
Lokaler Name2,5-Dimethoxybenzoylchlorid

Chemische & physikalische Eigenschaften

XLogP2,6
Polarare Oberfläche (TPSA)35,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren3
Frei drehbare Bindungen3
Schwere Atome13
Formalladung0
Komplexität184
Schmelzpunkt53-54 °C(Solv: ligroine (8032-32-4))
Siedepunkt179°C/10mm
Dichte1.224±0.06 g/cm3(Predicted)
CAS Datenbank17918-14-8(CAS DataBase Reference)

Sicherheit & Vorschriften

GHS-EinstufungDangerH314 (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.
Hazard Classes and CategoriesSkin Corr. 1B (100%)
Zollcode2918999090

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.