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Chemical Structure| 107112-93-6 Chemical Structure| 107112-93-6

Structure of 107112-93-6

Chemical Structure| 107112-93-6

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Product Details of [ 107112-93-6 ]

CAS No. :107112-93-6
Formula : C7H7NS
M.W : 137.20
SMILES Code : C1(C=CS2)=C2CCN=C1

Safety of [ 107112-93-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 107112-93-6 ]

* 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 [ 107112-93-6 ]

[ 107112-93-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 271-34-1 ]
  • [ 107112-93-6 ]
  • 3-(4,5,6,7-tetrahydrothieno[3,2-c]pyridin-4-yl)-5-azaindole [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With toluene-4-sulfonic acid; In neat (no solvent); at 100℃; for 2h;Microwave irradiation; the mixture of the cyclic imine 3,4-dihydroisoquinoline (66 mg, 0.50 mmol);6,7-dihydrothieno[3,2-c]pyridine (51 mg, 0.38 mmol); 3,4-dihydro--carboline (63 mg, 0.38 mmol) or4,5-dihydro-3H-benz[c]azepine (55.3 mg, 0.38 mmol); and the electron-rich aromatic compound (7-, 6-,4-, or <strong>[271-34-1]5-azaindole</strong> (30 mg, 0.25 mmol)) were placed in a 10 mL pressurized reaction vial and heated ina microwave reactor, under the conditions given in Tables 1-3. In the case of <strong>[271-34-1]5-azaindole</strong>, 10 mol % ofp-TSA (4.3 mg, 0.025 mmol) as a catalyst was also added.
 

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