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[ CAS No. 60230-37-7 ] {[proInfo.proName]}

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Chemical Structure| 60230-37-7
Chemical Structure| 60230-37-7
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Product Details of [ 60230-37-7 ]

CAS No. :60230-37-7 MDL No. :MFCD00729101
Formula : C6H5F2NO2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :RVVVGGCOFWWDEL-UHFFFAOYSA-N
M.W : 193.17 Pubchem ID :446274
Synonyms :

Safety of [ 60230-37-7 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338 UN#:1759
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 60230-37-7 ]

* 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 [ 60230-37-7 ]

[ 60230-37-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 88912-21-4 ]
  • [ 60230-37-7 ]
  • [ 204378-33-6 ]
YieldReaction ConditionsOperation in experiment
54.0% Synthesis Example 19 Synthesis of N-[(2,6-Difluorophenyl)sulfonyl]-6-chloro-4-methoxy-2-pyridinecarboxamide [Compound (I-975)] Using 2,6-difluorobenzenesulfonamide [Compound (III-14)] (0.309 g, 1.6 mmol) and 6-chloro-4-methoxypicolinic acid [Compound (II-75)] (0.3 g, 1.6 mmol), the Compound (I-975) was synthesised according to the process of Synthesis Example 3. White solid, yield: 0.3129 g, percent yield: 54.0%, m.p.: 160-163 C. IR KBr cm-1: 3262, 1725, 1620, 1434, 1398, 1317, 1188, 1029, 891, 642. 1H-NMR (60 MHz, CDCl3, 6): 3.8 (3H, s, OCH3), 6.7-7.5 (4H, m, aromatic ring H*3, pyridine ring H), 7.43 (1H, d, J=2 Hz, pyridine ring H), NH indistinctness.
  • 2
  • [ 26163-07-5 ]
  • [ 60230-37-7 ]
  • C13H13F2N3O2S [ No CAS ]
  • 3
  • [ 60230-37-7 ]
  • [ 13788-92-6 ]
  • C15H11F2N3O2S [ No CAS ]
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