2,3-Pyrazinecarboxylic anhydride

• CAS: 4744-50-7
• Catalog Number: ACM4744507
• Category: Polymer/Macromolecule
• Molecular Weight: 150.09
• Molecular Formula: C₆H₂N₂O₃
• Synonyms: PYRAZINE-2,3-DICARBOXYLIC ANHYDRIDE;2,3-PYRAZINEDICARBOXYLIC ANHYDRIDE;2,3-PYRAZINECARBOXYLIC ANHYDRIDE;FURO[3,4-B]PYRAZINE-5,7-DIONE;2,3-Pyrazinedicarboxylic acid anhydride;Furo[3,4-b]pyrazine-5,7-dione (9CI);2,3-PYRAZINEDICARBOXLIC ANHYDRIDE;2,3-PYRAZIN

Custom Q&A

What is the molecular formula of 2,3-Pyrazinecarboxylic anhydride?

The molecular formula of 2,3-Pyrazinecarboxylic anhydride is C6H2N2O3.

What is the molecular weight of 2,3-Pyrazinecarboxylic anhydride?

The molecular weight of 2,3-Pyrazinecarboxylic anhydride is 150.09 g/mol.

What is the IUPAC name of 2,3-Pyrazinecarboxylic anhydride?

The IUPAC name of 2,3-Pyrazinecarboxylic anhydride is furo[3,4-b]pyrazine-5,7-dione.

What is the InChI of 2,3-Pyrazinecarboxylic anhydride?

The InChI of 2,3-Pyrazinecarboxylic anhydride is InChI=1S/C6H2N2O3/c9-5-3-4(6(10)11-5)8-2-1-7-3/h1-2H.

What is the InChIKey of 2,3-Pyrazinecarboxylic anhydride?

The InChIKey of 2,3-Pyrazinecarboxylic anhydride is AWJWCTOOIBYHON-UHFFFAOYSA-N.

What is the canonical SMILES of 2,3-Pyrazinecarboxylic anhydride?

The canonical SMILES of 2,3-Pyrazinecarboxylic anhydride is C1=CN=C2C(=N1)C(=O)OC2=O.

What is the CAS number of 2,3-Pyrazinecarboxylic anhydride?

The CAS number of 2,3-Pyrazinecarboxylic anhydride is 4744-50-7.

What is the European Community (EC) number of 2,3-Pyrazinecarboxylic anhydride?

The European Community (EC) number of 2,3-Pyrazinecarboxylic anhydride is 225-260-4.

What is the DSSTox Substance ID of 2,3-Pyrazinecarboxylic anhydride?

The DSSTox Substance ID of 2,3-Pyrazinecarboxylic anhydride is DTXSID20197143.

Is 2,3-Pyrazinecarboxylic anhydride canonicalized?

Yes, 2,3-Pyrazinecarboxylic anhydride is canonicalized.

Synthetic Use

Upstream Synthesis Route 1

• 89-01-0
• 108-24-7

• 4744-50-7

Reference: [1] Molecules, 2017, vol. 22, # 9,
[2] Journal of the American Chemical Society, 1953, vol. 75, p. 679
[3] Helvetica Chimica Acta, 1958, vol. 41, p. 498,509

Downstream Synthesis Route 1

• 4744-50-7

• 98-96-4

Reference: [1] Yakugaku Zasshi, 1956, vol. 76, p. 470[2] Chem.Abstr., 1956, p. 14777

Downstream Synthesis Route 2

• 4744-50-7

• 6164-79-0

Reference: [1] Journal of the American Chemical Society, 1953, vol. 75, p. 679
[2] Yakugaku Zasshi, 1956, vol. 76, p. 470[3] Chem.Abstr., 1956, p. 14777

Downstream Synthesis Route 3

• 67-56-1
• 4744-50-7

• 73763-86-7

Reference: [1]Synthetic Communications,1996,vol. 26,p. 617 - 622
[2]Bioorganic and Medicinal Chemistry,2012,vol. 20,p. 6097 - 6108
[3]Journal of the American Chemical Society,1953,vol. 75,p. 679
[4]Patent: WO2012/9553,2012,A1 .Location in patent: Page/Page column 43; 44

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