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Chemical Structure| 25369-78-2 Chemical Structure| 25369-78-2
Chemical Structure| 25369-78-2

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Product Details of Tyrosinase-IN-22

CAS No. :25369-78-2
Formula : C7H5ClN2S
M.W : 184.65
SMILES Code : SC1=NC2=CC=C(Cl)C=C2N1
MDL No. :MFCD01044385
InChI Key :ZZIHEYOZBRPWMB-UHFFFAOYSA-N
Pubchem ID :2056429

Safety of Tyrosinase-IN-22

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of Tyrosinase-IN-22

* 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 [ 25369-78-2 ]

[ 25369-78-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3381-87-1 ]
  • [ 25369-78-2 ]
  • 5-chloro-2-(2-benzyloxybenzylthio)benzimidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
12% General procedure: Methanesulfonyl chloride (41 μL, 0.53 mmol) was dropwisely added to a solution of commercial 2-phenethylbenzylalcohol (75 mg, 0.35 mmol), triethylamine (98 μL, 0.70 mmol) and 4-dimethylaminopyridine (43 mg, 0.35 mmol) in CH2Cl2 (5 mL) at 0C. After the mixture was stirred overnight under Ar atmosphere, DMF (5 mL) solution of commercial 2-mercaptothiazoline (63 mg, 0.53 mmol), potassium iodide (58 mg, 0.35 mmol) and N,N-ethyldiisopropylamine (122 μL, 0.70 mmol) was added. After stirring at 100 C overnight, the reaction mixture was quenched with water, extracted with EtOAc, dried over MgSO4 and evaporated. The resulting residue was purified by column chromatography on silica gel (hexane/EtOAc = 6/1) to provide the title compound (20 mg, 0.064 mmol) as a yellow oil in 18% yield.
 

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