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Chemical Structure| 1226-42-2 Chemical Structure| 1226-42-2
Chemical Structure| 1226-42-2

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4,4'-Dimethoxybenzil is a human intestinal carboxyl esterase (hiCE) inhibitor with Ki of 70 nM.

Synonyms: p-Anisil

4.5 *For Research Use Only !

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Product Details of 4,4'-Dimethoxybenzil

CAS No. :1226-42-2
Formula : C16H14O4
M.W : 270.28
SMILES Code : O=C(C1=CC=C(OC)C=C1)C(C2=CC=C(OC)C=C2)=O
Synonyms :
p-Anisil
MDL No. :MFCD00008405
InChI Key :YNANGXWUZWWFKX-UHFFFAOYSA-N
Pubchem ID :71043

Safety of 4,4'-Dimethoxybenzil

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 4,4'-Dimethoxybenzil

* 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 [ 1226-42-2 ]

[ 1226-42-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 54523-47-6 ]
  • [ 1226-42-2 ]
  • [ 870249-44-8 ]
YieldReaction ConditionsOperation in experiment
90% With potassium hydroxide; In ethanol; at 70℃; for 3h;Inert atmosphere; (2) Intermediate product 2 (3.69 g, 10 mmol), 4,4'-dimethoxyphenol ester (Compound 3) (2.7 g, 10 mmol) and potassium hydroxide (0.168 g, 3 mmol) were added to the reaction flask, pumped three times, and solvent ethanol (30mL) was injected under nitrogen protection. The resulting mixture was refluxed at 70 C for three hours. After completion of the reaction, the reaction flask was cooled in an ice bath and precipitated to obtain the product. The product was washed with cold ethanol and dried to give red powder product 4 (compound 4). Yield 90%.
  • 3
  • [ 4506-66-5 ]
  • [ 1226-42-2 ]
  • [ 1227468-71-4 ]
  • 4
  • [ 7474-78-4 ]
  • [ 1226-42-2 ]
  • [ 1394971-68-6 ]
YieldReaction ConditionsOperation in experiment
80% In ethanol; water;Reflux; Step 2. 2,3-Bis-(4-methoxyphenyl)quinoxaline-6-sulfonic acid A solution of 1,2-bis(4-methoxyphenyl)ethane-1,2-dione (400 mg, 1.48 mmol, 1.00 equiv) and <strong>[7474-78-4]3,4-diaminobenzenesulfonic acid</strong> (278 mg, 1.48 mmol, 1.00 equiv) in ethanol/water (1:1, 20 mL) was stirred overnight at reflux in an oil bath. The resulting mixture was concentrated in vacuo, resulting in 500 mg (80percent) of 2,3-bis-(4-methoxyphenyl)quinoxaline-6-sulfonic acid as a brown solid.
80% In ethanol; water;Reflux; A solution of 1,2-bis(4-methoxyphenyl)ethane-1,2-dione (400 mg, 1.48 mmol, 1.00 equiv) and <strong>[7474-78-4]3,4-diaminobenzenesulfonic acid</strong> (278 mg, 1.48 mmol, 1.00 equiv) in ethanol/water (10/10 mL) was stirred overnight at reflux in an oil bath. The resulting mixture was concentrated under vacuum, yielding 500 mg (80percent) of 2,3-bis(4-methoxyphenyl)quinoxaline-6-sulfonic acid as a brown solid.
  • 5
  • [ 105-13-5 ]
  • [ 4903-09-7 ]
  • [ 1226-42-2 ]
 

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