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Chemical Structure| 884-35-5 Chemical Structure| 884-35-5
Chemical Structure| 884-35-5

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Methyl Syringate is a natural product with a unique inhibitory activity toward aflatoxin production, found in the herbs of Illicium micranthum.

Synonyms: Syringic Acid Methyl Ester

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Product Details of Methyl syringate

CAS No. :884-35-5
Formula : C10H12O5
M.W : 212.20
SMILES Code : O=C(OC)C1=CC(OC)=C(O)C(OC)=C1
Synonyms :
Syringic Acid Methyl Ester
MDL No. :MFCD00017199
InChI Key :ZMXJAEGJWHJMGX-UHFFFAOYSA-N
Pubchem ID :70164

Safety of Methyl syringate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H319
Precautionary Statements:P305+P351+P338

Application In Synthesis of Methyl syringate

* 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 [ 884-35-5 ]

[ 884-35-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 884-35-5 ]
  • [ 2478-38-8 ]
  • 2
  • [ 19064-24-5 ]
  • [ 884-35-5 ]
  • [ 866082-30-6 ]
YieldReaction ConditionsOperation in experiment
99% With caesium carbonate; In DMF (N,N-dimethyl-formamide); at 80℃; for 16h; To a solution of methylsyringate (1.0 g; 4.72 mmol) in DMF (50 mL) were added Cs2CO3 (1.85 g; 5.66 mmol) and 2,6-difluoronitrobezene (0.5 mL; 4.72 mmol). The reaction mixture was heated to 80 C. for 16 h. The mixture was cooled and poured into water, then extracted with EtOAc (3×). The organic layers were combined and washed with water (1×) then brine (1×). The organic phase was dried (MgSO4), filtered and concentrated in vacuo giving 1.64 g (99%) of 1-1 which was used in the next reaction without further purification.
99% With caesium carbonate; In N,N-dimethyl-formamide; at 80℃; for 16h; Preparation of Intermediate 1-5; Step l; [0051] To a solution of methylsyringate (1.Og; 4.72 mmol) in DMF (50 niL) were added Cs2CO3 (1.85 g; 5.66 mmol) and 2,6-difluoronitrobezene (0.5 niL; 4.72 mmol). The reaction mixture was heated to 80 0C for 16 h. The mixture was cooled and poured into water, then extracted with EtOAc (3X). The organic layers were combined and washed with water (IX) then brine (IX). The organic phase was dried (MgSO4), filtered and concentrated in vacuo giving 1.64 g (99%) of 1-1 which was used in the next reaction without further purification.
 

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