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METHYL 5,6-DICHLORONICOTINATE

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Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name: METHYL 5,6-DICHLORONICOTINATE
CAS:56055-54-0
Purity:98% Package:1KG;5USD|1000KG;0.1USD
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:METHYL 5,6-DICHLORONICOTINATE
CAS:56055-54-0
Purity:99% Package:1kg
Company Name: career henan chemical co
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Products Intro: Product Name:Methyl 5,6-Dichloronicotinate
CAS:56055-54-0
Purity:99% Package:1g;1USD
Company Name: Shaanxi Dideu Medichem Co. Ltd
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Products Intro: Product Name:METHYL 5,6-DICHLORONICOTINATE
CAS:56055-54-0
Purity:99.0% Package:100g;1kg;5kg;25kg
Company Name: Neostar United (Changzhou) Industrial Co., Ltd.
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Products Intro: Product Name:Methyl 5,6-dichloronicotinate
CAS:56055-54-0
Purity:0.99 Remarks:1KG,5KG,25KG,200KG

METHYL 5,6-DICHLORONICOTINATE manufacturers

METHYL 5,6-DICHLORONICOTINATE Basic information
Product Name:METHYL 5,6-DICHLORONICOTINATE
Synonyms:3-pyridinecarboxylic acid, 5,6-dichloro-, methyl ester;Methyl 5,6-dichloropyridine-3-carboxylate;Methyl 5,6-dichloropyridine-3-carboxylate, 5,6-Dichloro-3-(methoxycarbonyl)pyridine;Methyl 5,6-dichloropyridine-3-carboxylate, 2,3-Dichloro-5-(methoxycarbonyl)pyridine;3W-0272;5,6-dichloro-3-pyridinecarboxylic acid methyl ester;METHYL 5,6-DICHLORONICOTINATE;ZINC00168870
CAS:56055-54-0
MF:C7H5Cl2NO2
MW:206.03
EINECS:200-258-5
Product Categories:
Mol File:56055-54-0.mol
METHYL 5,6-DICHLORONICOTINATE Structure
METHYL 5,6-DICHLORONICOTINATE Chemical Properties
Melting point 63-65°C
Boiling point 265.5±35.0 °C(Predicted)
density 1.426±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-2.84±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 2933399990
MSDS Information
METHYL 5,6-DICHLORONICOTINATE Usage And Synthesis
Synthesis
Methanol

67-56-1

5,6-Dichloronicotinic acid

41667-95-2

METHYL 5,6-DICHLORONICOTINATE

56055-54-0

1. 5,6-Dichloropyridine-3-carboxylic acid (5 g) and thionyl chloride (3.10 g) were dissolved in methanol (20 mL) and the reaction was stirred overnight at 25 °C. 2. Upon completion of the reaction, cold water (100 mL) was added to the mixture and the mixture was neutralized with saturated sodium bicarbonate solution to pH neutral. 3. The aqueous layer was extracted using dichloromethane (2 x 100 mL). 4. The organic layers were combined, dried with anhydrous sodium sulfate and filtered to remove the drying agent. 5. The filtrate was concentrated under reduced pressure to give 5,6-dichloronicotinic acid methyl ester (5 g) as a white solid. 6. dried with anhydrous sodium sulfate and filtered to remove the desiccant. 5. The filtrate was concentrated under reduced pressure to give methyl 5,6-dichloronicotinate (5 g) as a white solid. 6. Mass Spectrometry (ESI): theoretical value of 205 for C7H5Cl2NO2; measured 206 [M + H]. 7.

References[1] Patent: WO2008/7900, 2008, A1. Location in patent: Page/Page column 15; 26
[2] Patent: US2009/209540, 2009, A1. Location in patent: Page/Page column 15; 7
[3] Patent: WO2008/128968, 2008, A1. Location in patent: Page/Page column 51
[4] Journal of Medicinal Chemistry, 2006, vol. 49, # 12, p. 3719 - 3742
[5] Patent: WO2018/165385, 2018, A1. Location in patent: Paragraph 00391
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