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ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE

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Products Intro: Product Name:ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE
CAS:34127-22-5
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Products Intro: Product Name:Ethyl 3,6-dichloropyridazine-4-carboxylate
CAS:34127-22-5
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CAS:34127-22-5
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Products Intro: Product Name:3,6-Dichloropyridazine-4-carboxylic acid ethyl ester
CAS:34127-22-5
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Products Intro: Product Name:4-Pyridazinecarboxylicacid, 3,6-dichloro-, ethyl ester
CAS:34127-22-5

ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE manufacturers

ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE Basic information
Product Name:ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE
Synonyms:3,6-Dichloropyridazine-4-carboxylic acid ethyl ester;ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE;4-Pyridazinecarboxylic acid, 3,6-dichloro-, ethyl ester;ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE ISO 9001:2015 REACH;3,6-Dichloro-5-ethylpyridazine-4-carbaldehyde
CAS:34127-22-5
MF:C7H6Cl2N2O2
MW:221.04
EINECS:
Product Categories:
Mol File:34127-22-5.mol
ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE Structure
ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE Chemical Properties
Boiling point 364.2±37.0 °C(Predicted)
density 1.433±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka-3.52±0.10(Predicted)
AppearanceLight yellow to brown Solid-Liquid Mixture
Safety Information
MSDS Information
ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE Usage And Synthesis
Synthesis
Ethanol

64-17-5

3,6-Dichloropyridazine-4-carboxylic acid

51149-08-7

ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE

34127-22-5

To a suspension of 3,6-dichloropyridazine-4-carboxylic acid (15.0 g, 78 mmol) in tetrahydrofuran (THF, 150 mL) was sequentially added ethanol (18.15 mL, 311 mmol) and 4-dimethylaminopyridine (DMAP, 0.950 g, 7.77 mmol). 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC, 16.39 g, 85 mmol) was added in batches over 1 min, and mild exothermic phenomena were observed during the reaction. The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the mixture was transferred to a dispensing funnel and neutralized by adding saturated aqueous sodium bicarbonate (NaHCO3) solution (150 mL). The aqueous phase was extracted with ether (3×250 mL), and the combined organic phases were washed with saturated saline (100 mL), dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: 20%→40% ethyl acetate/hexane solution; amount of silica gel: 300 g) to afford ethyl 3,6-dichloro-4-pyridazine-carboxylate (13.2 g, 59.7 mmol, 77% yield) as a colorless oil. The product was characterized as follows: 1H NMR (400 MHz, CDCl3) δ 7.88 (s, 1H), 4.50 (q, J = 7.0 Hz, 2H), 1.46 (t, J = 7.2 Hz, 3H); LCMS (ESI) m/e 221.1 [(M + H)+, theoretical value 221.0 (C7H7Cl2N2O2)].

References[1] Patent: WO2018/98411, 2018, A1. Location in patent: Page/Page column 20; 21; 23; 24; 68; 69
[2] Patent: WO2008/130951, 2008, A1. Location in patent: Page/Page column 81
[3] Journal of Medicinal Chemistry, 1993, vol. 36, # 18, p. 2676 - 2688
[4] Patent: WO2008/130600, 2008, A2. Location in patent: Page/Page column 70
[5] Patent: WO2004/108707, 2004, A1. Location in patent: Page 53-54
Tag:ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE(34127-22-5) Related Product Information
3,6-Dichloropyridazine-4-carboxylic acid 3,6-Dichloropyridazine 3,6-dichloro-4-pyridazinecarboxaldehyde Methyl 3,6-dichloropyridazine-4-carboxylate SALOR-INT L349488-1EA 3,6-Dichloro-4-methylpyridazine ETHYL 3,6-DICHLOROPYRIDAZINE-4-CARBOXYLATE Pyridazine-4-carboxylic acid methyl ester 3-Chloro-5-methylpyridazine ETHYL 4-PYRIDAZINECARBOXYLATE

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