Ethyl imidazole-4-carboxylate, 98%
Ethyl imidazole-4-carboxylate, 98%
Ethyl imidazole-4-carboxylate, 98%
Thermo Scientific Chemicals

Ethyl imidazole-4-carboxylate, 98%

CAS: 23785-21-9 | C6H8N2O2 | 140.14 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
Catalog number H64095.06
also known as H64095-06
Price (USD)
72.65
Special offer
Online exclusive
Ends: 30-Jun-2026
85.60
Save 12.95 (15%)
Each
Quantity:
5 g
Request bulk or custom format
Price (USD)
72.65
Special offer
Online exclusive
Ends: 30-Jun-2026
85.60
Save 12.95 (15%)
Each
Chemical Identifiers
CAS23785-21-9
IUPAC Nameethyl 1H-imidazole-5-carboxylate
Molecular FormulaC6H8N2O2
InChI KeyKLWYPRNPRNPORS-UHFFFAOYSA-N
SMILESCCOC(=O)C1=CN=CN1
View more
SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)>97.5%
A ring-substituted-1H-imidazole-4-carboxylic acid derivative, that is shown to act as a new class of anti-tuberculosis agents.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
A ring-substituted-1H-imidazole-4-carboxylic acid derivative, that is shown to act as a new class of anti-tuberculosis agents.

Solubility
Soluble in dimethyl sulfoxide and methanol. Slightly soluble in water.

Notes
Refrigerate. Keep container tightly closed. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Preeti Gupta; Shahul Hameed; Rahul Jain. Ring-substituted imidazoles as a new class of anti-tuberculosis agents. J. Phys. Chem.20049(39), 805-814.
  2. P. Dan Cook; Robert J. Rousseau; A. Mohsin Mian; Phoebe Dea; Rich B. MeyerJr.; Roland K. Robins. Synthesis of 3-deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid by a novel ring closure of imidazole precursors. J. Am. Chem. Soc. 197698(6), 805-814.