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[ CAS No. 53553-05-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 53553-05-2
Chemical Structure| 53553-05-2
Structure of 53553-05-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 53553-05-2 ]

CAS No. :53553-05-2 MDL No. :MFCD06660592
Formula : C7H3Cl3O4S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 289.52 Pubchem ID :-
Synonyms :

Safety of [ 53553-05-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338 UN#:3261
Hazard Statements:H318 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 53553-05-2 ]

* 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 [ 53553-05-2 ]

[ 53553-05-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 53553-05-2 ]
  • [ 584-08-7 ]
  • 3-(N-Butylsulfonamidoyl)-2,6-dichlorobenzoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With N-butylamine In toluene 33.B 3-(N-Butylsulfonamidoyl)-2,6-dichlorobenzoic acid and Other Compound of Formula 3 Part B: 3-(Chlorosulfonyl)-2,6-dichlorobenzoic acid (1.5 g; 5.2 mmol) was dissolved in anhydrous toluene (35 ml) to which was added powdered K2 CO3 (1.44 g: 10.4 mmol) and n-butylamine (1.0 ml, 10.4 mmol). The reaction mixture was stirred at 25° C. for 12 hours. The solution was diluted slowly with 1 M ethereal HCl (20 ml) and was then stirred for 30 minutes. The solution was filtered and the resulting filtrate was evaporated to dryness to give crude product. Further purification of the material by silica gel chromatography using EtOAc as the eluent provided 3-N-butylsulfonamidoyl)-2,6-dichlorobenzoic acid (Formula 3) (1.43 g, 85%. 1 H NMR (DMSO) d 8.11 (t, 1H), 7.98 and 7.71 (doublets, 1H each), 2.75 (m, 2H), 1.55 (m, 2H), 1.32 (m 2H), 0.87 (t, 3H)
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