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Chemical Structure| 937-62-2 Chemical Structure| 937-62-2

Structure of 937-62-2

Chemical Structure| 937-62-2

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Product Details of [ 937-62-2 ]

CAS No. :937-62-2
Formula : C8H7ClO2
M.W : 170.59
SMILES Code : O=C(Cl)OC1=CC=C(C)C=C1
MDL No. :MFCD00013255

Safety of [ 937-62-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H311+H331-H314
Precautionary Statements:P261-P270-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Class:6.1(8)
UN#:3277
Packing Group:

Application In Synthesis of [ 937-62-2 ]

* 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 [ 937-62-2 ]

[ 937-62-2 ] Synthesis Path-Downstream   1~1

  • 1
  • rac-(1RS,2RS)-1-amino-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-2-ol [ No CAS ]
  • [ 101601-80-3 ]
  • [ 937-62-2 ]
  • rac-1-((1R,2R)-2-hydroxy-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-yl)-3-(2-phenylpyridin-3-yl)urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
26 mg Synthesis of rac-1-((1R,2R)-2-hydroxy-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-yl)-3-(2-phenylpyridin-3-yl)urea To an acetonitrile (0.50 mL) solution of commercially available 2-phenyl-3-pyridineamine (CAS number 101601-80-3) (25 mg), p-tolyl chloroformate (25 mg) was added. After stirring the reaction solution at room temperature for 1 hour, triethylamine (0.061 mL) and the compound (31 mg) obtained in (Example 1) <Step 4> were added to the reaction solution, followed by stirring at 40 C. for 3 hours. The reaction solution was purified by preparative LC-Mass to obtain the title compound (26 mg).
 

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