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Chemical Structure| 7163-50-0 Chemical Structure| 7163-50-0

Structure of 7163-50-0

Chemical Structure| 7163-50-0

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Product Details of [ 7163-50-0 ]

CAS No. :7163-50-0
Formula : C9H8O3
M.W : 164.16
SMILES Code : O=C(O)C(C1=CC=C(C)C=C1)=O
MDL No. :MFCD00961859
InChI Key :UIIIPQVTXBPHTI-UHFFFAOYSA-N
Pubchem ID :151451

Safety of [ 7163-50-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 7163-50-0 ]

* 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 [ 7163-50-0 ]

[ 7163-50-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 7163-50-0 ]
  • [ 137-07-5 ]
  • [ 16112-21-3 ]
YieldReaction ConditionsOperation in experiment
75% With trimethyl-(2-hydroxyethyl)ammonium chloride; tartaric acid; at 60℃; for 0.5h; 1) Take a 10mL Erlenmeyer flask or test tube, add 0.2mmol 2-aminothiophenol, 0.4mmol p-toluoyl formic acid and 2mL deep eutectic solvent (the molar ratio of choline chloride to tartaric acid is 2: 1 );(2) Place the Erlenmeyer flask or test tube in step (1) into a 60 C oil bath and stir magnetically for 30 min to obtain the crude product;(3) Separate the crude product obtained in step (2) by column chromatography. The eluent is a mixture of ethyl acetate and petroleum ether.The volume ratio is 1: 6, and it is dried at 30 C for 3 hours to obtain a 2-arylbenzothiazole compound.
73% at 60℃; for 0.5h;Green chemistry; General procedure: (a) Deep eutectic solvent synthesis: Choline chloride and the hydrogen bond donor (urea, oxalic acid, zinc chloride, etc.) were placed into a 10 mL plugged test tube. The reagents were mixed evenly, then heated and stirred in an 80 C oil bath until a uniform and transparent liq- uid was ready for use (generally 30 min). (b) Synthesis of cyclization product: o-Substituted aniline (0.30 mmol) and -keto acid (0.45 mmol) and DES (1 mL) were allowed to react in an oil bath at 80 C for 2.0 h. The reaction mixture was then extracted with EtOAc (5 ×), organic phases were combined, distilled and con- centrated to obtain the crude product, and then separated by column chromatography to obtain the pure product.
  • 2
  • [ 7163-50-0 ]
  • [ 24316-19-6 ]
  • C27H27NO6 [ No CAS ]
  • 3
  • [ 7163-50-0 ]
  • [ 1141-88-4 ]
  • [ 16112-21-3 ]
  • 4
  • [ 7163-50-0 ]
  • [ 446065-11-8 ]
  • methyl 2-cyclohexyl-2-hydroxy-2-(p-tolyl)acetate [ No CAS ]
  • 5
  • [ 7163-50-0 ]
  • [ 446065-11-8 ]
  • [ 94204-03-2 ]
 

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