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Structure

2-Oxiranecarboxylic acid

CAS
4538-50-5
Catalog Number
ACM4538505
Category
Main Products
Molecular Weight
88.06
Molecular Formula
C3H4O3

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Specification

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
Canonical 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
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".

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.

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