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Chemical Structure| 88353-04-2 Chemical Structure| 88353-04-2

Structure of 88353-04-2

Chemical Structure| 88353-04-2

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Product Details of [ 88353-04-2 ]

CAS No. :88353-04-2
Formula : C19H28O4
M.W : 320.42
SMILES Code : O=C(OCC1=CC=CC=C1)CCCCCCCCCCC(O)=O
MDL No. :MFCD29090558
InChI Key :ZDTVBXVYNIHVNR-UHFFFAOYSA-N
Pubchem ID :14250267

Safety of [ 88353-04-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 88353-04-2 ]

* 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 [ 88353-04-2 ]

[ 88353-04-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 623-57-4 ]
  • [ 88353-04-2 ]
  • 1,12-dodecanedioic acid benzyl ester 2-(11-benzyloxycarbonylundecanoyloxy)-3-dimethylaminopropyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
50% With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20℃; for 48h; Dodecanedioic acid benzyl ester 2-(11-benzyloxycarbonyl-undecanoyloxy)-3-dimethylamino-propyl ester (29a) To an ice-cold solution of 24a (1.78 g, 5.5 mmol), 3-dimethylamino-propane-1,2-diol (0.3 mL, 2.5 mmol) and DMAP (catalytic amount) in DCM (15 mL) was slowly added a solution of DCC (1.1 g, 5.5 mmol) in DCM (5 mL). After the addition, the solution was warmed to room temperature and stirred for 2 days. The reaction mixture was then filtered to remove the insoluble DCU. Concentration of the filtrate followed by chromatography (50percent EtOAc/DCM to 100percent EtOAC) afforded 0.9 g (50percent yield) product as colorless oil. The characterization data were consistent with the proposed structure.
  • 2
  • [ 623-57-4 ]
  • [ 88353-04-2 ]
  • [2,3-bis-(11-benzyloxycarbonylundecanoyloxy)propyl]trimethylammonium iodide [ No CAS ]
 

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