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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 887266-97-9 Chemical Structure| 887266-97-9

Structure of 887266-97-9

Chemical Structure| 887266-97-9

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Product Details of [ 887266-97-9 ]

CAS No. :887266-97-9
Formula : C7H6ClFO3S
M.W : 224.64
SMILES Code : O=S(C1=CC=C(F)C(OC)=C1)(Cl)=O
MDL No. :MFCD07368708

Safety of [ 887266-97-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H312-H314-H332
Precautionary Statements:P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 887266-97-9 ]

* 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 [ 887266-97-9 ]

[ 887266-97-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 58196-33-1 ]
  • [ 887266-97-9 ]
  • 7-((2-chloro-6-fluorobenzyl)oxy)-1-((4-fluoro-3-methoxyphenyl)sulfonyl)-1,2,3,4-tetrahydroquinoline [ No CAS ]
  • 2
  • [ 58196-33-1 ]
  • [ 887266-97-9 ]
  • 1-[(4-fluoro-3-methoxybenzene)sulfonyl]-1,2,3,4-tetrahydroquinolin-7-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
7.0 g With pyridine; In dichloromethane; at 20℃; for 1h; j00410j To a solution of <strong>[58196-33-1]1,2,3,4-tetrahydroquinolin-7-ol</strong> (2.5 g, 16.76 mmol) indichloromethane (100 mL) was added pyridine (2.6 g, 32.9 mmol) and 4-fluoro-3-methoxybenzene-1-sulfonyl chloride (5.6 g, 24.93 mmol, 1.50 equiv). The mixture was stirred for one hour at room temperature. Then, methanol (2 mL) was added to the reaction mixture, and the resulting mixture was concentrated to provide a residue. The residue was purified via MPLC eluting with dichloromethane/ethyl acetate (2:1) to afford 1-[(4-fluoro-3-methoxybenzene)sulfonyl]-<strong>[58196-33-1]1,2,3,4-tetrahydroquinolin-7-ol</strong> (7.0 g) as a red oil.
7 g With pyridine; In dichloromethane; at 20℃; for 1h; To a solution of <strong>[58196-33-1]1,2,3,4-tetrahydroquinolin-7-ol</strong> (2.5 g, 16.76 mmol) in dichloromethane (100 mL) was added pyridine (2.6 g, 32.9 mmol) and 4-fluoro-3- methoxybenzene-1-sulfonyl chloride (5.6 g, 24.93 mmol, 1.50 equiv). The mixture was stirred for one hour at room temperature. Then, methanol (2 mL) was added to the reaction mixture, and the resulting mixture was concentrated to provide a residue. The residue was purified via MPLC eluting with dichloromethane/ethyl acetate (2:1) to afford 1-[(4-fluoro-3- methoxybenzene)sulfonyl]-<strong>[58196-33-1]1,2,3,4-tetrahydroquinolin-7-ol</strong> (7.0 g) as a red oil.
 

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