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65001-21-0

65001-21-0 Structure

65001-21-0 Structure
IdentificationBack Directory
[Name]

5-BROMOPYRIDINE-3-SULFONYL CHLORIDE
[CAS]

65001-21-0
[Synonyms]

5-Bromopyridin-3-sulfonyl chloride
5-bromo-3-pyridinesulfonyl chloride
3-Bromo-5-(chlorosulphonyl)pyridine
5-BROMOPYRIDINE-3-SULFONYL CHLORIDE
5-Bromo-3-(chlorosulphonyl)pyridine
5-BROMOPYRIDINE-3-SULPHONYL CHLORIDE
3-Pyridinesulfonyl chloride, 5-broMo-
5-Bromopyridine-3-sulphonylchloride97%
5-Bromopyridine-3-sulphonyl chloride 97%
5-BROMOPYRIDINE-3-SULFONYL CHLORIDE ISO 9001:2015 REACH
[Molecular Formula]

C5H3BrClNO2S
[MDL Number]

MFCD08235263
[MOL File]

65001-21-0.mol
[Molecular Weight]

256.5
Chemical PropertiesBack Directory
[Melting point ]

60-62.5
[Boiling point ]

329.2±27.0 °C(Predicted)
[density ]

1.893±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-4.09±0.21(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C5H3BrClNO2S/c6-4-1-5(3-8-2-4)11(7,9)10/h1-3H
[InChIKey]

AVILRJQPDYPXFQ-UHFFFAOYSA-N
[SMILES]

C1=NC=C(Br)C=C1S(Cl)(=O)=O
[CAS DataBase Reference]

65001-21-0
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310
[Hazard Codes ]

C,Xi
[Risk Statements ]

14-20/21/22-29-34-36
[Safety Statements ]

8-22-26-30-36/37/39-45
[RIDADR ]

2923
[Hazard Note ]

Corrosive
[HazardClass ]

8
[PackingGroup ]

Ⅲ
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMOPYRIDINE-3-SULFONYL CHLORIDE(65001-21-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-BROMOPYRIDINE-3-SULPHONIC ACID 96

62009-34-1

5-BROMOPYRIDINE-3-SULFONYL CHLORIDE

65001-21-0

General procedure for the synthesis of 5-bromopyridine-3-sulfonyl chloride from 5-bromopyridine-3-sulfonic acid: a mixture of 5-bromopyridine-3-sulfonic acid (7.14 g, 30 mmol), phosphorus pentachloride (9.68 g, 47 mmol), and phosphorus trichloride (20 mL) was heated to reflux, and the reaction was carried out for 4 h. (Ref: J. Org. Chem. 1989, 54(2) , 389). Upon completion of the reaction, the mixture was concentrated to dryness to give a yellow semi-solid. The semi-solid was dissolved in a solvent mixture of ice water and tert-butyl methyl ether, and saturated aqueous NaHCO3 solution was added slowly until neutralized. Subsequently, the organic and aqueous phases were separated by saturating the solution with solid NaCl. The organic phase was dried with anhydrous Na2SO4. Finally, the solvent was removed in vacuum to give a yellow solid 5-bromopyridine-3-sulfonyl chloride (7.57 g, 98% yield). The mass spectrum (EI) showed m/z of 254.9 [M+], 256.9 [M+2]+, and 258.9 [M+4]+; the melting point was 64 °C. The analytes were analyzed in aqueous phase and in the presence of aqueous phase.

[References]

[1] Patent: US2006/217387, 2006, A1. Location in patent: Page/Page column 26
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