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Pyridine-3-sulfonyl chloride hydrochloride

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Products Intro: Product Name:Pyridine-3-sulfonyl chloride
CAS:42899-76-3
Purity:98% (Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:Pyridine-3-sulfonyl chloride hydrochloride
CAS:42899-76-3
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CAS:42899-76-3
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Products Intro: Product Name:Pyridine-3-sulfonyl chloride hydrochloride
CAS:42899-76-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-04210

Pyridine-3-sulfonyl chloride hydrochloride manufacturers

Pyridine-3-sulfonyl chloride hydrochloride Basic information
Product Name:Pyridine-3-sulfonyl chloride hydrochloride
Synonyms:TIMTEC-BB SBB010621;Pyridine-3-sulphonyl chloride hydrochloride, tech;Pyridine-3-sulfonylchlorideHCl;ASINEX-REAG BAS 13031029;Pyridine-3-sulfonyl chloride hydrochloride ,95%;Pyridine-3-sulfonyl chlor...;Pyridine-3-Sulphonyl Chloride Hcl;3-(Chlorosulphonyl)pyridine hydrochloride
CAS:42899-76-3
MF:C5H5Cl2NO2S
MW:214.07
EINECS:
Product Categories:Heterocycle-Pyridine series;blocks;Pyridines
Mol File:42899-76-3.mol
Pyridine-3-sulfonyl chloride hydrochloride Structure
Pyridine-3-sulfonyl chloride hydrochloride Chemical Properties
Melting point 120-126
Fp >110℃
storage temp. Inert atmosphere,Store in freezer, under -20°C
Appearancewhite solid
Water Solubility Reacts with water.
Sensitive Moisture Sensitive
Safety Information
Hazard Codes C
Risk Statements 14-29-34
Safety Statements 8-22-26-30-45-36/37/39
RIDADR UN 3265 8 / PGII
Hazard Note Corrosive/Keep Cold under -20C
HazardClass IRRITANT
HazardClass 8
HS Code 29333990
MSDS Information
Pyridine-3-sulfonyl chloride hydrochloride Usage And Synthesis
Chemical PropertiesWhite solid
Synthesis
3-Pyridinesulfonic acid

636-73-7

Pyridine-3-sulfonyl chloride hydrochloride

42899-76-3

General procedure for the synthesis of pyridine-3-sulfonyl chloride hydrochloride from 3-pyridinesulfonic acid: 3-pyridinesulfonic acid (3.00 g, 18.8 mmol) was mixed with phosphorus pentachloride (PCl5, 4.79 g, 23.0 mmol) in phosphorus oxychloride (POCl3, 6 mL). The reaction mixture was stirred and reacted at 120°C overnight (15 h). After completion of the reaction, it was cooled to room temperature, diluted with chloroform (CHCl3, 20 mL) and saturated with hydrogen chloride gas (HCl(g)). The precipitated white precipitate was collected by filtration, washed with chloroform and dried under reduced pressure to give the title compound pyridine-3-sulfonyl chloride hydrochloride (3.36 g, 83% yield) as a white powder.

References[1] Advanced Synthesis and Catalysis, 2004, vol. 346, # 8, p. 925 - 928
[2] Patent: WO2008/3703, 2008, A1. Location in patent: Page/Page column 82
[3] Patent: US2007/60623, 2007, A1. Location in patent: Page/Page column 24
[4] Patent: WO2006/36024, 2006, A1. Location in patent: Page/Page column 160
[5] Patent: EP2336107, 2015, B1. Location in patent: Paragraph 0306
Pyridine-3-sulfonyl chloride hydrochloride Preparation Products And Raw materials
Raw materialsPhosphorus oxitrichloride-->Pyridine-->FUMING SULFURIC ACID-->MERCURY(II) SULFATE-->3-Pyridinesulfonic acid-->Chloroform-->Hydrochloric acid
Preparation Products3-Pyridinesulfonamide-->5-phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde
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