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N-METHOXYCARBONYLMALEIMIDE

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N-METHOXYCARBONYLMALEIMIDE Basic information

Product Name:
N-METHOXYCARBONYLMALEIMIDE
Synonyms:
  • N-METHOXYCARBONYLMALEIMIDE
  • 106271
  • methyl 2,5-dihydro-2,5-dioxo-1H-pyrrole-1-carboxylate
  • 2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-carboxylic acid methyl ester
  • 2,5-Dioxo-2,5-dihydro-1H-pyrrole-1-carboxylic acid methyl ester
  • 2,5-Dioxo-3-pyrroline-1-carboxylic acid methyl ester
  • Einecs 259-792-3
  • N-(CarboMethoxy)MaleiMide
CAS:
55750-48-6
MF:
C6H5NO4
MW:
155.11
EINECS:
259-792-3
Product Categories:
  • Building Blocks
  • Carbonyl Compounds
  • Chemical Synthesis
  • Cyclic Imides
  • Organic Building Blocks
  • Life Science Chemical Reagents
  • Nitric Oxide Reagents
  • Cross Linking Reagents
  • Maleimide Derivatives
  • MTS & Sulfhydryl Active Reagents
  • Carbonyl Compounds
  • Cyclic Imides
  • Organic Building Blocks
Mol File:
55750-48-6.mol
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N-METHOXYCARBONYLMALEIMIDE Chemical Properties

Melting point:
63-65 °C
Boiling point:
242.5±23.0 °C(Predicted)
Density 
1.496±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
solubility 
DMSO (Slightly), Ethyl Acetate (Slightly), Chloroform
form 
Solid
pka
-3.17±0.20(Predicted)
color 
Off-White to Pink
BRN 
1450638
InChI
InChI=1S/C6H5NO4/c1-11-6(10)7-4(8)2-3-5(7)9/h2-3H,1H3
InChIKey
LLAZQXZGAVBLRX-UHFFFAOYSA-N
SMILES
N1(C(OC)=O)C(=O)C=CC1=O
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
10
HS Code 
29251900

MSDS

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N-METHOXYCARBONYLMALEIMIDE Usage And Synthesis

Chemical Properties

Off-White Cyrstalline Solid

Uses

N-(Methoxycarbonyl) Maleimide (cas# 55750-48-6) is a compound useful in organic synthesis.

Synthesis

541-59-3

79-22-1

55750-48-6

To a solution of ethyl acetate (120 mL) of maleimide (6.35 g, 65.4 mmol) was sequentially added N-methylmorpholine (NMM, 8.6 mL, 78.5 mmol) and methyl chloroformate (6.0 mL, 78.5 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 30 min, then brought to room temperature and continued stirring for 1 h. The reaction was completed by filtration. Upon completion of the reaction, the solid was collected by filtration and the filtrate was concentrated under reduced pressure. The concentrated residue was dissolved in dichloromethane, filtered through a silica gel column and eluted with dichloromethane to remove red impurities. The eluate was concentrated and the resulting solid was ground with a solvent mixture of ethyl acetate and petroleum ether to give a final white solid of methyl 2,5-dioxo-2,5-dihydro-1H-pyrrole-1-carboxylate (9.0 g, 88% yield).

References

[1] Chemistry Letters, 2012, vol. 41, # 3, p. 313 - 315
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 20, p. 7890 - 7901
[3] Patent: WO2017/46658, 2017, A1. Location in patent: Page/Page column 149; 150
[4] Journal of Fluorine Chemistry, 2013, vol. 152, p. 173 - 181
[5] Journal of the American Chemical Society, 2008, vol. 130, # 34, p. 11288 - 11289

N-METHOXYCARBONYLMALEIMIDE Preparation Products And Raw materials

Raw materials

N-METHOXYCARBONYLMALEIMIDESupplier

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