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Chemical Structure| 166964-26-7 Chemical Structure| 166964-26-7

Structure of 166964-26-7

Chemical Structure| 166964-26-7

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Product Details of [ 166964-26-7 ]

CAS No. :166964-26-7
Formula : C6H7ClO3S
M.W : 194.64
SMILES Code : CC1=CC(=C(C)O1)S(Cl)(=O)=O
MDL No. :MFCD04115370

Safety of [ 166964-26-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H335
Precautionary Statements:P260-P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 166964-26-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 166964-26-7 ]

[ 166964-26-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 166964-26-7 ]
  • [ 33084-49-0 ]
  • N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With NaH; In tetrahydrofuran; B. N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide was prepared by the method of Example 41 with 4-bromo-3-methyl-5-amino-isoxazole (2.0 mmoles, 0.35 g), NaH (5.0 mmoles, 200 mg), 2,5-dimethyl-furan-3-sulfonylchloride (2.4 mmoles, 0.47 g) and THF (9 ml). Flash chromatography (5% methanol/chloroform) followed by recrystallization from chloroform and hexanes provided 0.21 g (31%) of a light brown solid, m.p. 85.5-87 C.
With NaH; In tetrahydrofuran; B. N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide was prepared by the method of Example 41 with 4-bromo-3-methyl5-amino-isoxazole (2.0 mmoles, 0.35 g), NaH (5.0 mmoles, 200 mg), 2,5-dimethyl-furan-3-sulfonylchloride (2.4 mmoles, 0.47 g) and THF (9 ml). Flash chromatography (5% methanol/chloroform) followed by recrystallization from chloroform and hexanes provided 0.21 g (31%) of a light brown solid, m.p. 85.5-87 C.
  • 2
  • [ 166964-26-7 ]
  • [ 33084-49-0 ]
  • N-(4-bromo-3-methyl-5-isoxazolyl)-2,5-dimethyl-furan-3-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% With NaH; B. Furan-2-sulfonyl chloride Furan-2-sulfonyl chloride was prepared by the method of Example 1 with 4-bromo-3-methyl-2-aminoisoxazole (0.354 g, 2.0 mmol), NaH (60% oil dispersion) (200 g, 5.0 mmol) and 2,5-dimethylfuran 3-sulfonyl chloride (0.467 g, 2.4 mmol). Flash chromatography (5% CH3 OH/CHCl3) and recrystallization from CHCl3 /hexane provided 0.21 4 g (32% yield) of light brown crystals (m.p. 85.5-87 C.).
 

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