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Chemical Structure| 153203-57-7 Chemical Structure| 153203-57-7

Structure of 153203-57-7

Chemical Structure| 153203-57-7

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Product Details of [ 153203-57-7 ]

CAS No. :153203-57-7
Formula : C9H7ClO4
M.W : 214.60
SMILES Code : O=C(O)C1=CC(C(OC)=O)=CC(Cl)=C1
MDL No. :MFCD08458982

Safety of [ 153203-57-7 ]

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 [ 153203-57-7 ]

* 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 [ 153203-57-7 ]

[ 153203-57-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 28179-47-7 ]
  • [ 153203-57-7 ]
YieldReaction ConditionsOperation in experiment
47% With n-Butyl nitrite; copper dichloride; In acetonitrile; at 0 - 20℃; for 2.0h; 2.5 g (18.6 mmol) copper-(II)-chloride and 3.6 ml (30.8 mmol) n-butylnitrite were dissolved in 50 ml acetonitrile. While cooling with the ice bath a suspension of 3.0 g (15.4 mmol) 6.3-a in 150 ml acetonitrile was slowly metered in and the reaction solution was stirred for 2 hours at ambient temperature. After the reaction had ended the mixture was evaporated down i. vac., the residue was combined with dichloromethane and washed with 3N HCl and water. The organic phase was evaporated to dryness using the rotary evaporator, the residue was combined with diethyl ether, the precipitate was filtered off and dried. Yield 1.6 g (47%) beige crystals 9-a. ES-MS (M+H)+=215
 

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