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Chemical Structure| 2756-87-8 Chemical Structure| 2756-87-8
Chemical Structure| 2756-87-8

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MMF can induce Nrf2 activation.

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Product Details of Monomethyl fumarate

CAS No. :2756-87-8
Formula : C5H6O4
M.W : 130.10
SMILES Code : O=C(O)/C=C/C(OC)=O
MDL No. :MFCD00063174
InChI Key :NKHAVTQWNUWKEO-NSCUHMNNSA-N
Pubchem ID :5369209

Safety of Monomethyl fumarate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313

Application In Synthesis of Monomethyl fumarate

* 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 [ 2756-87-8 ]

[ 2756-87-8 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 2756-87-8 ]
  • [ 24316-19-6 ]
  • [ 61568-73-8 ]
  • 2
  • [ 5835-79-0 ]
  • [ 2756-87-8 ]
  • [ 1448896-52-3 ]
YieldReaction ConditionsOperation in experiment
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0℃; Example 16 Preparation of the MMF Prodrug Methyl 4-morpholin-4-ylbutyl (2E)but-2-ene-1,4-dioate Methyl 4-morpholin-4-ylbutyl (2E)but-2-ene-1,4-dioate Monomethyl fumarate (MMF) was reacted with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDAC) (1.2 eq) in dichloromethane (DCM) at ca. 0 C. 4-Morpholin-4-yl-butan-1-ol (1 eq) and 4-N,N-dimethylaminopyridine (DMAP) (catalytic amount) were added to the activated carboxylic acid. After the completion of the reaction, followed by the work-up of the reaction mixture, the title compound was isolated as a viscous-oil.
  • 3
  • [ 2756-87-8 ]
  • [ 1202759-91-8 ]
  • C24H24FN5O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
62% Weigh 29mgMonomethyl fumarate,84mg HATU, 30mg HOAT in a 25ml round bottom flask, add 1.6mlDCM, 0.4 ml DMF and 66 mul DIEA were used as solvents. After stirring at room temperature for about 10 minutes, 74 mg of the A1 intermediate was added to the reaction system. After stirring for about 1 hour at room temperature, 100 ml of saturated aqueous sodium bicarbonate solution was added, followed by 15 ml of DCM. The mixture was extracted 3 times and the organic phase was evaporated to dryness under reduced pressure. The residue was applied to a silica gel column with DCM:MeOH=70:1 (volume ratio) to obtain 60 mg of the compound represented by Formula I-2 in a yield of 62%
  • 4
  • [ 2756-87-8 ]
  • [ 67630-01-7 ]
  • [ 693-13-0 ]
  • C28H44N4O8 [ No CAS ]
  • 5
  • [ 2756-87-8 ]
  • [ 67630-01-7 ]
  • [ 538-75-0 ]
  • C34H52N4O8 [ No CAS ]
  • 6
  • [ 2756-87-8 ]
  • [ 1118749-75-9 ]
  • [ 67630-01-7 ]
  • C34H48N4O9 [ No CAS ]
  • 7
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  • C11H20N2O2 [ No CAS ]
  • [ 67630-01-7 ]
  • C32H50N4O10 [ No CAS ]
  • 8
  • [ 2756-87-8 ]
  • [ 67630-01-7 ]
  • tert-Butyl-pentyl-carbodiimide [ No CAS ]
  • C31H50N4O8 [ No CAS ]
  • 9
  • [ 2756-87-8 ]
  • C12H23N3O2 [ No CAS ]
  • [ 67630-01-7 ]
  • C33H53N5O10 [ No CAS ]
  • 10
  • [ 2756-87-8 ]
  • C18H22N2 [ No CAS ]
  • [ 67630-01-7 ]
  • C39H52N4O8 [ No CAS ]
  • 11
  • [ 2756-87-8 ]
  • [ 1202-53-5 ]
  • [ 67630-01-7 ]
  • C32H50N4O8 [ No CAS ]
  • 12
  • [ 2756-87-8 ]
  • [ 63540-08-9 ]
  • [ 67630-01-7 ]
  • C30H46N4O8 [ No CAS ]
  • 13
  • [ 2756-87-8 ]
  • [ 67630-01-7 ]
  • [ 197635-71-5 ]
  • C36H44N4O9 [ No CAS ]
 

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