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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
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Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 1122-97-0 Chemical Structure| 1122-97-0

Structure of 1122-97-0

Chemical Structure| 1122-97-0

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Product Details of [ 1122-97-0 ]

CAS No. :1122-97-0
Formula : C7H8S2
M.W : 156.26
SMILES Code : SC1=CC=C(SC)C=C1
MDL No. :MFCD00082770

Safety of [ 1122-97-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H311+H331-H315-H319
Precautionary Statements:P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 1122-97-0 ]

* 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 [ 1122-97-0 ]

[ 1122-97-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 53595-65-6 ]
  • [ 1122-97-0 ]
  • [ 63031-87-8 ]
  • 2
  • [ 1122-97-0 ]
  • [ 252019-48-0 ]
  • [ 43156-47-4 ]
YieldReaction ConditionsOperation in experiment
Chem., 1975, 18, 1164 for the preparation of 2-nitro-5-phenylsulphanylaniline but using 4-methylsulphanylthiophenol in place of thiophenol) was added portionwise over 5 minutes and the mixture was stirred a further 2 hours at 0° C., allowed to warm to ambient temperature, and stirred a further 16 hours. Volatile material was removed by evaporation and the residue was purified by flash chromatography on silica gel eluding with 10-30percent ethyl acetate/hexane to give the title compound (4.5 g) as a solid. NMR (CDCl3) 2.52 (s, 3H), 7.03-7.08 (m, 1H), 7.3 (d, 2H), 7.36-7.38 (m, 1H), 7.44 (d, 2H), 7.77 (d, 1H).
 

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