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Chemical Structure| 198623-55-1 Chemical Structure| 198623-55-1

Structure of 198623-55-1

Chemical Structure| 198623-55-1

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Product Details of [ 198623-55-1 ]

CAS No. :198623-55-1
Formula : C12H16O4
M.W : 224.25
SMILES Code : O=C(OC)C1=CC(OCC)=CC(OCC)=C1
MDL No. :MFCD12025085
InChI Key :TWYWKJRUBYVESZ-UHFFFAOYSA-N
Pubchem ID :53961617

Safety of [ 198623-55-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330

Application In Synthesis of [ 198623-55-1 ]

* 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 [ 198623-55-1 ]

[ 198623-55-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 124480-95-1 ]
  • [ 18107-18-1 ]
  • [ 198623-55-1 ]
  • 2
  • [ 198623-55-1 ]
  • [ 124480-95-1 ]
YieldReaction ConditionsOperation in experiment
With lithium hydroxide; In tetrahydrofuran; water; The mono-alkylation of compound 12.2 is conducted by the treatment of 12.2 and NaH in DMF. Halide RDX (1 eq) is added to the reaction mixture to afford the corresponding aryl ether 12.3. The second alkylation is performed under the some conditions with halide REX [(1] eq), followed by basic hydrolysis (LiOH, [H20/THF)] to give acid 12.1 as the intermediate for use in making compounds like those described in Example 44. Illustrative examples of suitable halides and their corresponding final products are shown in Table 13.
With lithium hydroxide; water; In tetrahydrofuran; This example describes the synthesis of compounds of the formula wherein RD and RE are each independently substituted or unsubstituted aliphatic or aromatic moieties. These compounds are prepared according to Scheme 8 and the procedure below. Compound 8.2 is treated with NaH in DMF, and halide RDX (1 eq) is added to the reaction mixture to yield aryl ether 8.3. Compound 8.3 is then treated with NaH in DMF, and halide REX (1 eq) is added. The reaction mixture is hydrolized (LiOH, H2O/THF) to give acid 8.1. Compounds 8.1, acids of the formula RCCOOH, are used to make additional compounds of the invention. Table 4 shows exemplary compounds 8.1's.
 

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