2-Quinoxalinecarboxylic acid methyl ester

• CAS: 1865-11-8
• Catalog Number: ACM1865118
• Category: Other Products
• Molecular Weight: 188.18272
• Molecular Formula: C₁₀H₈N₂O₂
• Synonyms: 2-Quinoxalinecarboxylic acid methyl ester;-Quinoxalinecarboxylic acid Methyl ester;Methyl quinoxaline-2-carboxylate;QCA-Methyl ester

Custom Q&A

What is the molecular formula of 2-Quinoxalinecarboxylic acid methyl ester?

The molecular formula of 2-Quinoxalinecarboxylic acid methyl ester is C10H8N2O2.

What is the chemical structure of 2-Quinoxalinecarboxylic acid methyl ester?

The chemical structure of 2-Quinoxalinecarboxylic acid methyl ester is not provided in the reference.

What are the synonyms for 2-Quinoxalinecarboxylic acid methyl ester?

The synonyms for 2-Quinoxalinecarboxylic acid methyl ester are:
Methyl quinoxaline-2-carboxylate
1865-11-8
Quinoxaline-2-carboxylic acid methyl ester
Methyl 2-quinoxalinecarboxylate

What is the molecular weight of 2-Quinoxalinecarboxylic acid methyl ester?

The molecular weight of 2-Quinoxalinecarboxylic acid methyl ester is 188.18 g/mol.

When was 2-Quinoxalinecarboxylic acid methyl ester created?

2-Quinoxalinecarboxylic acid methyl ester was created on March 27, 2005.

What is the IUPAC name of 2-Quinoxalinecarboxylic acid methyl ester?

The IUPAC name of 2-Quinoxalinecarboxylic acid methyl ester is methyl quinoxaline-2-carboxylate.

What is the InChI of 2-Quinoxalinecarboxylic acid methyl ester?

The InChI of 2-Quinoxalinecarboxylic acid methyl ester is InChI=1S/C10H8N2O2/c1-14-10(13)9-6-11-7-4-2-3-5-8(7)12-9/h2-6H,1H3.

What is the InChIKey of 2-Quinoxalinecarboxylic acid methyl ester?

The InChIKey of 2-Quinoxalinecarboxylic acid methyl ester is KDPBLDOVCGAWNQ-UHFFFAOYSA-N.

What is the Canonical SMILES of 2-Quinoxalinecarboxylic acid methyl ester?

The Canonical SMILES of 2-Quinoxalinecarboxylic acid methyl ester is COC(=O)C1=NC2=CC=CC=C2N=C1.

What is the XLogP3 value of 2-Quinoxalinecarboxylic acid methyl ester?

The XLogP3 value of 2-Quinoxalinecarboxylic acid methyl ester is 2.

Synthetic Use

Upstream Synthesis Route 1

• 67-56-1
• 819868-69-4

• 5182-90-1
• 1865-11-8

Reference: [1] Synlett, 2004, # 13, p. 2323 - 2326

Upstream Synthesis Route 2

• 67-56-1
• 819868-68-3

• 5182-90-1
• 1865-11-8

Reference: [1] Synlett, 2004, # 13, p. 2323 - 2326

Downstream Synthesis Route 1

• 1865-11-8

• 5182-90-1

Reference: [1] Supramolecular Chemistry, 2015, vol. 27, # 11-12, p. 780 - 786
[2] Patent: WO2018/116072, 2018, A1, . Location in patent: Page/Page column 74
[3] Pharmaceutical bulletin, 1957, vol. 5, # 3, p. 277 - 279
[4] Journal of Medicinal Chemistry, 2002, vol. 45, # 25, p. 5604 - 5606

Downstream Synthesis Route 2

• 1865-11-8

• 5182-90-1

Reference: [1]Supramolecular Chemistry,2015,vol. 27,p. 780 - 786
[2]Patent: WO2018/116072,2018,A1 .Location in patent: Page/Page column 74
[3]Pharmaceutical bulletin,1957,vol. 5,p. 277 - 279
[4]Journal of Medicinal Chemistry,2002,vol. 45,p. 5604 - 5606

Downstream Synthesis Route 3

• 1865-11-8

• 114354-19-7

Reference: [1]Pharmaceutical bulletin,1957,vol. 5,p. 277 - 279

Downstream Synthesis Route 4

• 1865-11-8

• 54571-06-1

Reference: [1]Journal of Medicinal Chemistry,2002,vol. 45,p. 5604 - 5606
[2]Pharmaceutical bulletin,1957,vol. 5,p. 277 - 279

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