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[ CAS No. 34981-38-9 ] {[proInfo.proName]}

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Chemical Structure| 34981-38-9
Chemical Structure| 34981-38-9
Structure of 34981-38-9 * Storage: {[proInfo.prStorage]}
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Product Details of [ 34981-38-9 ]

CAS No. :34981-38-9 MDL No. :MFCD09742738
Formula : C7H6Cl2O2S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 225.09 Pubchem ID :-
Synonyms :

Safety of [ 34981-38-9 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3265
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 34981-38-9 ]

* 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 [ 34981-38-9 ]

[ 34981-38-9 ] Synthesis Path-Downstream   1~4

  • 2
  • [ 34981-38-9 ]
  • [ 479-50-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: zinc-powder; aqueous H2SO4 2: water 3: sulfuric acid 4: pyridine / 180 °C
Multi-step reaction with 4 steps 1: zinc-powder; aqueous H2SO4 2: K2CO3; copper-powder; KI / weiteres Reagens: Benzylalkohol 3: sulfuric acid 4: pyridine / 180 °C
  • 3
  • [ 1101120-05-1 ]
  • [ 34981-38-9 ]
  • [ 302-15-8 ]
  • [ 1353889-40-3 ]
YieldReaction ConditionsOperation in experiment
46% General procedure: These were made using NaHCO3 or 2,6-lutidine as detailed below, unless otherwise stated. Methylhydrazine sulfate (1.2 equiv) and NaHCO3 (5 equiv) were added to a solution of <strong>[1101120-05-1]3-formylpyrazolo[1,5-a]pyridine-5-carbonitrile</strong> (2) (1 equiv) in MeOH (5 mL). After all of the aldehyde was consumed, sulfonyl chloride or acyl chloride (1.3 equiv) was added and the reaction mixture stirred for a further 30 min. The solvent was removed in vacuo and the residue taken up in CH2Cl2 and water. The layers were separated and the aqueous phase extracted with CH2Cl2, then the combined organic layers were dried (Na2SO4) and the solvent removed in vacuo. Chromatography or trituration then afforded the hydrazides. Alternatively, methylhydrazine sulfate (1.2 equiv) and 2,6-lutidine (5 equiv) were added to a solution of 2 (1 equiv) in MeOH (5 mL). After all of the aldehyde was consumed, sulfonyl chloride or acyl chloride (1.3 equiv) was added and the reaction mixture stirred for a further 30 min. The hydrazide was then filtered off, washed with MeOH and dried.
  • 4
  • [ 34981-38-9 ]
  • [ 26638-53-9 ]
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