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Chemical Structure| 93300-54-0 Chemical Structure| 93300-54-0

Structure of 93300-54-0

Chemical Structure| 93300-54-0

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Product Details of [ 93300-54-0 ]

CAS No. :93300-54-0
Formula : C14H10ClN3S
M.W : 287.77
SMILES Code : SC1=NN=C(C2=CC=C(Cl)C=C2)N1C3=CC=CC=C3
MDL No. :MFCD00298451
InChI Key :AJOJIGWGJWZBOB-UHFFFAOYSA-N
Pubchem ID :736518

Safety of [ 93300-54-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 93300-54-0 ]

* 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 [ 93300-54-0 ]

[ 93300-54-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 93300-54-0 ]
  • [ 17329-87-2 ]
  • 2-((5-(4-chlorophenyl)-4-phenyl-4H-1,2,4-triazol-3-yl)thio)-N-(4-nitrophenyl)acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% General procedure: Synthetic procedure was performed in oven-dried flat bot- tom flask enabled with a Teflon-coated magnetic stirring bar, rubber septa and nitrogen balloon. It was charged with 5- (4-chlorophenyl)-4-phenyl-4 H -1,2,4-triazole-3-thiol (1.0 mmol) in 20 mL tetrahydrofuran followed by dropwise addition of tri- ethyl amine (1.0 mmol) in stirring condition. After few minutes sui table 2 -chloro- N -phenylacetamide derivative (1.0 mmol) was added and reflux for 5-8 hours. Reaction completion was con- cluded by TLC in Ethyl acetate: Hexane (40:60). Reaction mixture was quenched by pouring it into cold water. Crude product was filtered and washed with ice water (3 ×20 mL). Precipitates were dried in oven at 48 C temp to remove bound water molecules. Pu- rification was achieved by crystallization in hot methanol, results in characteristic shaped pure crystalline product.
 

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