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Chemical Structure| 1701-24-2 Chemical Structure| 1701-24-2

Structure of 1701-24-2

Chemical Structure| 1701-24-2

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Product Details of [ 1701-24-2 ]

CAS No. :1701-24-2
Formula : C10H5ClF3N
M.W : 231.60
SMILES Code : FC(C1=NC2=CC=CC=C2C(Cl)=C1)(F)F
MDL No. :MFCD00153105
InChI Key :ONNDFDQMHCNEGF-UHFFFAOYSA-N
Pubchem ID :2736709

Safety of [ 1701-24-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1701-24-2 ]

* 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 [ 1701-24-2 ]

[ 1701-24-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 1701-24-2 ]
  • [ 629-30-1 ]
  • [ 372-31-6 ]
  • [ 124467-00-1 ]
  • [ 1701-18-4 ]
YieldReaction ConditionsOperation in experiment
With aniline; In PPA; B2 (2E/Z, 4E) N-Isobutyl 3-methyl-11-(2-trifluoromethyl-4-quinolinyloxy)undeca-2,4-dienamide Starting from 2-trifluoromethyl-4-chloroquinoline and 1,7-heptanediol. Ethyl trifluoroacetoacetate (3.7 g) and aniline (1.8 ml) were reacted together in polyphosphoric acid according to Joullie et al, J. Med. Chem., 16, 134 (1973), to give 2-trifluoromethyl-4-hydroxyquinoline (1.8 g).
 

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