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Chemical Structure| 3463-02-3 Chemical Structure| 3463-02-3

Structure of 3463-02-3

Chemical Structure| 3463-02-3

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Product Details of [ 3463-02-3 ]

CAS No. :3463-02-3
Formula : C8H11NS
M.W : 153.24
SMILES Code : NC1=CC=C(SCC)C=C1
MDL No. :MFCD00040310

Safety of [ 3463-02-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H315-H319-H331-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P311-P330-P361-P363-P403+P233-P405-P501
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 3463-02-3 ]

* 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 [ 3463-02-3 ]

[ 3463-02-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 110-81-6 ]
  • [ 62-53-3 ]
  • [ 3463-02-3 ]
  • [ 13920-91-7 ]
  • 2
  • [ 624-89-5 ]
  • [ 622-37-7 ]
  • [ 3463-02-3 ]
  • [ 13920-91-7 ]
  • [ 2987-53-3 ]
  • [ 104-96-1 ]
  • 3
  • [ 352-93-2 ]
  • [ 622-37-7 ]
  • [ 3463-02-3 ]
  • [ 13920-91-7 ]
  • 4
  • [ 14290-92-7 ]
  • [ 622-37-7 ]
  • [ 3463-02-3 ]
  • [ 13920-91-7 ]
  • 5
  • [ 3240-35-5 ]
  • [ 3463-02-3 ]
  • 4-ethylthio-N-(4-sulfamoylbenzylidene)aniline [ No CAS ]
YieldReaction ConditionsOperation in experiment
56% 85(i) 4-Ethylthio-N-(4-sulfamoylbenzylidene)aniline Following a procedure similar to that described in Example 1(i), but using 4-sulfamoylbenzaldehyde and 4-ethylthioaniline as starting materials, the title compound was obtained as a yellow powder (yield 56%). Nuclear Magnetic Resonance Spectrum (270 MHz, hexadeuterated dimethyl sulfoxide) δ ppm: 8.76 (1H, singlet); 8.10 (2H, doublet, J=8 Hz); 7.95 (2H, doublet, J=8 Hz); 7.50 (2H, singlet); 7.40-7.30 (4H, multiplet); 3.01 (2H, quartet, J=7 Hz); 1.27-1.22 (3H, multiplet).
 

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