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Chemical Structure| 215437-47-1 Chemical Structure| 215437-47-1

Structure of 215437-47-1

Chemical Structure| 215437-47-1

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Product Details of [ 215437-47-1 ]

CAS No. :215437-47-1
Formula : C12H10ClNO
M.W : 219.67
SMILES Code : ClC1=CN=C(OCC2=CC=CC=C2)C=C1
MDL No. :MFCD11976459
InChI Key :SXOVMWQGOMWDHU-UHFFFAOYSA-N
Pubchem ID :10932953

Safety of [ 215437-47-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-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 [ 215437-47-1 ]

* 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 [ 215437-47-1 ]

[ 215437-47-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4214-79-3 ]
  • [ 100-44-7 ]
  • [ 215437-47-1 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N-methyl-acetamide; nitrogen; ethyl acetate; toluene; 2 Synthesis of 2-Benzyloxy-5-chloropyridine: In a reaction flask were charged 10 g of <strong>[4214-79-3]5-chloro-2-hydroxypyridine</strong>, 11.73 g of benzyl chloride, 16 g of potassium carbonate, and 250 ml of dimethylformamide in a nitrogen stream, and the mixture was reacted at 80° C. for 2 hours. After cooling, the organic layer was filtered, and the salt was washed with ethyl acetate and filtered. The solvent was evaporated, and the residue was purified by column chromatography using 150 g of silica gel and a 5:1 (by volume) mixture of toluene and ethyl acetate as a developing solvent to give 14.5 g of the title compound.
  • 2
  • O-benzyl S-prop-2-yn-1-yl carbonodithioate [ No CAS ]
  • [ 4214-79-3 ]
  • [ 215437-47-1 ]
 

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