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Chemical Structure| 1383546-18-6 Chemical Structure| 1383546-18-6

Structure of 1383546-18-6

Chemical Structure| 1383546-18-6

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Product Details of [ 1383546-18-6 ]

CAS No. :1383546-18-6
Formula : C5H4INO2S
M.W : 269.06
SMILES Code : O=C(C1=C(I)SN=C1C)O
MDL No. :MFCD28140500

Safety of [ 1383546-18-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1383546-18-6 ]

* 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 [ 1383546-18-6 ]

[ 1383546-18-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15903-66-9 ]
  • [ 1383546-18-6 ]
YieldReaction ConditionsOperation in experiment
General procedure: To a solution of 3-methylisothiazole-4-carboxylic acid (E-4) (3.9 g, 27.3 mmol) in anhydrousTHF (150 mL) at -78 C under argon, n-butyllithium solution (27.3 mL, 68.3 mmol) is added dropwise and the resulting mixture is stirred at -78 C for 1 h. To this mixture, a solution of iodide (13.9 g, 54.6 mmol) in THF (50 mL) is added slowly and the resulting mixture is stirred at RT for 1 h. The mixture is acidified with concentrated HCl to adjust the pH to 3-4, and then extracted with ethyl acetate. The organic layer is washed with aqueous Na2S03 solution. The aqueous layer is extracted with ethyl acetate. The combined organic layers are washed with brine, dried over Na2S04 and filtered. The filtrate is concentrated in vacuo to afford the product, 5-iodo-3-methylisothiazole-4-carboxylic acid (E-5).
To a solution of 3-methylisothiazole-4-carboxylic acid (G-4) (3.9 g, 27.3 mmol) in anhydrousTHF (150 mL) at -78 C under argon, n-butyl lithium solution (27.3 mL, 68.3 mmol) is added dropwise and the resulting mixture is stirred at -78 C for 1 h. To this mixture, a solution of iodide (13.9 g, 54.6 mmol) in THF (50 mL) is added slowly and the resulting mixture is stirred at RT for 1 h. The mixture is acidified with concentrated HC1 to adjust the pH to 3-4, and then extracted with ethyl acetate. The organic layer is washed with aqueous Na2S03 solution. The aqueous layer is extracted with ethyl acetate. The combined organic layers are washed with brine, dried over Na2S04 and filtered. The filtrate is concentrated in vacuo to afford the product, 5-iodo-3- methylisothiazole-4-carboxylic acid (G-5).
General procedure: To a solution of 3-methylisothiazole-4-carboxylic acid (C-4) (3.9 g, 27.3 mmol) in anhydrous THF (150 mL) at -78 C. under argon, n-butyl lithium solution (27.3 mL, 68.3 mmol) is added dropwise and the resulting mixture is stirred at -78 C. for 1 h. To this mixture, a solution of iodine (13.9 g, 54.6 mmol) in THF (50 mL) is added slowly and the resulting mixture is stirred at RT for 1 h. The mixture is acidified with concentrated HCl to adjust the pH to 3-4, and then extracted with ethyl acetate. The organic layer is washed with aqueous Na2SO3 solution. The aqueous layer is extracted with ethyl acetate. The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo to afford the product, 5-iodo-3-methylisothiazole-4-carboxylic acid (C-5).
 

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