2-Oxiranecarboxylic acid

• CAS: 4538-50-5
• Catalog Number: ACM4538505
• Category: Main Products
• Molecular Weight: 88.06
• Molecular Formula: C₃H₄O₃
• Synonyms: Glycidic acid methyl ester, Methyl 2-oxiranecarboxylate, Oxiranecarboxylic acid, methyl ester, CID145751, Oxirane-2-carboxylic acid, methyl ester, 4538-50-5
• IUPAC Name: methyl oxirane-2-carboxylate
• SMILES: COC(=O)C1CO1
• InChI Key: YKNYRRVISWJDSR-UHFFFAOYSA-N
• Boiling Point: 97.4ºC at 760 mmHg
• Flash Point: 26.2ºC
• Density: 1.246g/cm³
• EC Number: 610-247-1
• Exact Mass: 102.03200
• H-Bond Acceptor: 3
• H-Bond Donor: 0

Custom Q&A

What is the molecular formula of 2-Oxiranecarboxylic acid?

The molecular formula of 2-Oxiranecarboxylic acid is C3H4O3.

What are the synonyms of 2-Oxiranecarboxylic acid?

The synonyms of 2-Oxiranecarboxylic acid are Oxirane-2-carboxylic acid, Glycidic acid, and Epoxypropionic acid.

What is the molecular weight of 2-Oxiranecarboxylic acid?

The molecular weight of 2-Oxiranecarboxylic acid is 88.06 g/mol.

What is the IUPAC name of 2-Oxiranecarboxylic acid?

The IUPAC name of 2-Oxiranecarboxylic acid is oxirane-2-carboxylic acid.

What is the InChI code for 2-Oxiranecarboxylic acid?

The InChI code for 2-Oxiranecarboxylic acid is InChI=1S/C3H4O3/c4-3(5)2-1-6-2/h2H,1H2,(H,4,5).

What is the InChIKey for 2-Oxiranecarboxylic acid?

The InChIKey for 2-Oxiranecarboxylic acid is OTGHWLKHGCENJV-UHFFFAOYSA-N.

What is the canonical SMILES representation of 2-Oxiranecarboxylic acid?

The canonical SMILES representation of 2-Oxiranecarboxylic acid is C1C(O1)C(=O)O.

What is the CAS number of 2-Oxiranecarboxylic acid?

The CAS number of 2-Oxiranecarboxylic acid is 503-11-7.

What is the European Community (EC) number of 2-Oxiranecarboxylic acid?

The European Community (EC) number of 2-Oxiranecarboxylic acid is 207-961-7.

What is the Wikipedia page for 2-Oxiranecarboxylic acid?

The Wikipedia page for 2-Oxiranecarboxylic acid is "Glycidic acid".

Synthetic Use

Downstream Synthesis Route 1

• 4538-50-5

• 18289-89-9
• 4538-50-5

Reference: [1] Tetrahedron, 2014, vol. 70, # 27-28, p. 4165 - 4180
[2] Journal of the American Chemical Society, 2002, vol. 124, # 7, p. 1307 - 1315
[3] Journal of the American Chemical Society, 2002, vol. 124, # 7, p. 1307 - 1315

Downstream Synthesis Route 2

• 4538-50-5

• 18289-89-9
• 10303-88-5
• 4538-50-5

Reference: [1] Journal of the American Chemical Society, 2002, vol. 124, # 7, p. 1307 - 1315
[2] Journal of the American Chemical Society, 2004, vol. 126, # 5, p. 1360 - 1362
[3] Advanced Synthesis and Catalysis, 2006, vol. 348, # 18, p. 2619 - 2625

Downstream Synthesis Route 3

• 4538-50-5

• 18289-89-9
• 10303-88-5
• 4538-50-5

Reference: [1] Journal of the American Chemical Society, 2002, vol. 124, # 7, p. 1307 - 1315

Downstream Synthesis Route 4

• 4538-50-5

• 51877-54-4

Reference: [1]Journal of Organic Chemistry,1992,vol. 57,p. 1029 - 1031

Downstream Synthesis Route 5

• 4538-50-5

• 18289-89-9
• 10303-88-5
• 4538-50-5

Reference: [1]Journal of the American Chemical Society,2002,vol. 124,p. 1307 - 1315
[2]Journal of the American Chemical Society,2004,vol. 126,p. 1360 - 1362
[3]Advanced Synthesis and Catalysis,2006,vol. 348,p. 2619 - 2625

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