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Chemical Structure| 502764-53-6 Chemical Structure| 502764-53-6

Structure of 502764-53-6

Chemical Structure| 502764-53-6

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Product Details of [ 502764-53-6 ]

CAS No. :502764-53-6
Formula : C10H4O4S3
M.W : 284.33
SMILES Code : O=C(C(S1)=CC2=C1C3=C(C=C(C(O)=O)S3)S2)O
InChI Key :XQMFYBSHBCPMBJ-UHFFFAOYSA-N
Pubchem ID :68324914

Safety of [ 502764-53-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 502764-53-6 ]

* 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 [ 502764-53-6 ]

[ 502764-53-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 502764-52-5 ]
  • [ 502764-53-6 ]
YieldReaction ConditionsOperation in experiment
88.2% With lithium hydroxide; In tetrahydrofuran; water; for 6.5h;Reflux; 152.0 g (0.446 mol) of the compound represented by the formula 3-c obtained from the above reaction formula 17 and 2.3 L of tetrahydrofuran were added to a 5 L round bottom flask, and then 95.5 g (2,277 mol) of lithium hydroxide was dissolved in 2.3 L of water, The reaction mixture was stirred for 30 minutes and then refluxed for 6 hours. After the temperature was lowered to room temperature, 3 L of 1 N hydrochloric acid was poured, and the solid was filtered, washed with methanol and dried to obtain 112.0 g (88.2%) of the compound represented by the formula 3-d.
 

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