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Chemical Structure| 48126-51-8 Chemical Structure| 48126-51-8

Structure of 48126-51-8

Chemical Structure| 48126-51-8

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Product Details of [ 48126-51-8 ]

CAS No. :48126-51-8
Formula : C10H10O2
M.W : 162.19
SMILES Code : O=C([C@H]1[C@@H](C2=CC=CC=C2)C1)O
MDL No. :MFCD06227614

Safety of [ 48126-51-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 48126-51-8 ]

* 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 [ 48126-51-8 ]

[ 48126-51-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 939-89-9 ]
  • [ 48126-51-8 ]
  • 2
  • ((1S)-2-formyl-cyclopropyl)-benzene [ No CAS ]
  • [ 23020-15-7 ]
  • [ 48126-51-8 ]
  • 3
  • [ 939-89-9 ]
  • [ 23020-18-0 ]
  • [ 48126-51-8 ]
YieldReaction ConditionsOperation in experiment
With Chiralpak AD-H; In methanol;Resolution of racemate; Commercially purchased ±<strong>[939-89-9]cis-2-phenylcyclopropanecarboxylic acid</strong> was separated into constituent enantiomers (Intermediate W and Y) using SFC (Chiralpak AD-H, C02/Methanol 8:2, 3 mL/min, 100 bar), Intermediate W was the first eluting isomer at Rt 2.31 min and intermediate X was second eluting isomer at Rt 2.89 min. The stereochemistry of Intermediates W and X was arbitrarily assigned.
 

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