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Chemical Structure| 530-56-3 Chemical Structure| 530-56-3
Chemical Structure| 530-56-3

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4-Hydroxy-3,5-dimethoxybenzyl alcohol is a 2,4,6-substituted phenol with antiviral properties.

Synonyms: 4-Hydroxy-3,5-dimethoxybenzyl alcohol; Syringic Alcohol

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Product Details of Syringyl Alcohol

CAS No. :530-56-3
Formula : C9H12O4
M.W : 184.19
SMILES Code : OCC1=CC(OC)=C(O)C(OC)=C1
Synonyms :
4-Hydroxy-3,5-dimethoxybenzyl alcohol; Syringic Alcohol
MDL No. :MFCD00016871
InChI Key :LUOAEJWSKPQLJD-UHFFFAOYSA-N
Pubchem ID :10741

Safety of Syringyl Alcohol

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

Application In Synthesis of Syringyl Alcohol

* 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 [ 530-56-3 ]

[ 530-56-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 6638-05-7 ]
  • [ 530-56-3 ]
  • 3
  • [ 6638-05-7 ]
  • [ 7732-18-5 ]
  • oxygen [ No CAS ]
  • enzyme-substance from mushrooms [ No CAS ]
  • [ 530-56-3 ]
  • [ 530-55-2 ]
  • [ 15640-40-1 ]
  • [ 134-96-3 ]
  • 4
  • [ 50-00-0 ]
  • [ 91-10-1 ]
  • [ 530-56-3 ]
  • [ 6638-05-7 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; COMPARATIVE EXAMPLE 1 310 g of 2,6-dimethoxyphenol, 300 g of 38 wtpercent formalin, and 810 g of 10percent wtpercent aqueous sodium hydroxide were reacted for 60 hours at 25° C. under a pressure of 0 kg/cm2 -G, the reaction mixture was and then neutralized with sulfuric acid, to obtain 80 g of 2,6-dimethoxy-4-(hydroxymethyl)phenol. (Yield: 22 molpercent) 25 g of the obtained 2,6-dimethoxy-4-(hydroxymethyl)phenol was reacted in 320 ml of methanol in the presence of 0.375 wtpercent of platinum-alumina catalyst and hydrogen for 4 hours at 200° C. at 199 kg/cm2 -G, and 15 g of 2,6-dimethoxy-4-methylphenol was obtained. (Yield: 66 molpercent) The yield on the basis of the amount of the raw material was 15 molpercent.
With sodium hydroxide; COMPARATIVE EXAMPLE 1 310g of 2,6-dimethoxyphenol, 300 g of 38 wtpercent formalin, and 810 g of 10 wtpercent aqueous sodium hydroxide were reacted for 60 hours at 25 °C under a pressure of 0 kg/cm2-G, the reaction mixture was and then neutralized with sulfuric acid, to obtain 80 g of 2,6-dimethoxy-4-(hydroxymethyl)phenol. (Yield: 22 molpercent) 25 g of the obtained 2,6-dimethoxy-4-(hydroxymethyl)phenol was reacted in 320 ml of methanol in the presence of 0.375 wtpercent of platinum-alumina catalyst and hydrogen for 4 hours at 200 °C at 199 kg/cm2-G, and 15 g of 2,6-dimethoxy-4-methylphenol was obtained. (Yield: 66 molpercent) The yield on the basis of the amount of the raw material was 15 molpercent.
 

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