N-(2-Hydroxyethyl)maleimide

• CAS: 1585-90-6
• Catalog Number: ACM1585906
• Category: Alcohols
• Molecular Weight: 141.12
• Molecular Formula: C₅H₁₂O₃
• Synonyms: 1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE;N-(2-HYDROXYETHYL)MALEIMIDE
• Density: 1.395 g/cm³
• Hazard Statements: H226-H319-H332
• RIDADR: NONH for all modes of transport
• Symbol: GHS02

Custom Q&A

What is the molecular formula of N-(2-Hydroxyethyl)maleimide?

The molecular formula is C6H7NO3.

What is the molecular weight of N-(2-Hydroxyethyl)maleimide?

The molecular weight is 141.12 g/mol.

What is the IUPAC name of N-(2-Hydroxyethyl)maleimide?

The IUPAC name is 1-(2-hydroxyethyl)pyrrole-2,5-dione.

What is the InChI of N-(2-Hydroxyethyl)maleimide?

The InChI is InChI=1S/C6H7NO3/c8-4-3-7-5(9)1-2-6(7)10/h1-2,8H,3-4H2.

What is the InChIKey of N-(2-Hydroxyethyl)maleimide?

The InChIKey is AXTADRUCVAUCRS-UHFFFAOYSA-N.

What is the Canonical SMILES of N-(2-Hydroxyethyl)maleimide?

The Canonical SMILES is C1=CC(=O)N(C1=O)CCO.

What is the CAS number of N-(2-Hydroxyethyl)maleimide?

The CAS number is 1585-90-6.

What is the European Community (EC) number of N-(2-Hydroxyethyl)maleimide?

The European Community (EC) number is 696-457-4.

What is the XLogP3 value of N-(2-Hydroxyethyl)maleimide?

The XLogP3 value is -0.1.

Is N-(2-Hydroxyethyl)maleimide considered as a canonicalized compound?

Yes, N-(2-Hydroxyethyl)maleimide is considered a canonicalized compound.

Synthetic Use

Upstream Synthesis Route 1

• 32620-90-9

• 1585-90-6

Reference: [1] Patent: WO2007/44169, 2007, A1, . Location in patent: Page/Page column 10

Upstream Synthesis Route 2

• 108-31-6
• 141-43-5

• 1585-90-6

Reference: [1] Archiv der Pharmazie, 2016, vol. 349, # 6, p. 466 - 474
[2] Patent: CN107162950, 2017, A, . Location in patent: Paragraph 0091-0093
[3] Farmaco, 2002, vol. 57, # 5, p. 421 - 426

Upstream Synthesis Route 3

• 1585-79-1

• 1585-90-6

Reference: [1] Macromolecules, 2004, vol. 37, # 1, p. 18 - 26

Downstream Synthesis Route 1

• 1585-90-6
• 358-23-6

• 155863-37-9

Reference: [1]Journal of Heterocyclic Chemistry,1994,vol. 31,p. 457 - 480
[2]Journal of Medicinal Chemistry,1994,vol. 37,p. 2609 - 2618

Downstream Synthesis Route 2

• 1585-90-6
• 7143-01-3

• 155863-36-8

Reference: [1]Patent: WO2012/12612,2012,A2 .Location in patent: Page/Page column 37

* For details of the synthesis route, please refer to the original source to ensure accuracy.