1-Methyl-1H-Imidazole-4,5-Dicarboxylic Acid(CAS 19485-38-2)
| Purity | Grade | Package | Stock | Price | Quantity |
| 98% | RG | 1G | In Stock | 5 USD
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| 98% | RG | 5G | In Stock | 14 USD
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| 98% | RG | 25G | In Stock | 46 USD
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| 98% | RG | 100G | In Stock | 184 USD
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| 98% | RG | 500G | In Stock | 1208 USD
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Applications of 19485-38-2
| Industry | Application | Process |
|---|---|---|
| Pharmaceutical Chemicals | Pharmaceutical Intermediates | Used to synthesize various imidazole-containing active pharmaceutical ingredients (APIs), such as antiparasitic and antifungal agents, via amidation or esterification to incorporate the target molecular structure. |
| Pharmaceutical Chemicals | Raw Material for Imidazole Derivative Synthesis | Serves as a key building block for constructing fused heterocyclic compounds—e.g., imidazopyridines and imidazoquinolines—applied in the development of anticancer or antiviral drugs. |
| Organometallic Chemistry (MOFs) | Ligand for Metal–Organic Frameworks (MOFs) | Acts as a polydentate ligand through its two carboxylic acid groups and the nitrogen atom on the imidazole ring, coordinating with metal ions (e.g., Zn, Cu, Co) to assemble MOF materials with defined pore structures via hydrothermal or solvothermal methods. |
| Organometallic Chemistry (MOFs) | Functional Material Preparation | Used to prepare porous materials exhibiting gas adsorption, separation, or catalytic properties, forming high-surface-area crystalline materials via coordination polymerization. |
| Coordination Chemistry | Metal Complex Synthesis | Functions as a chelating agent to form stable complexes with transition metals or lanthanides, applied in synthesizing fluorescent probes or catalyst precursors; crystals are typically obtained via solution evaporation or diffusion methods. |
| Biochemistry | Bioactive Molecule Design | Employed to synthesize structural analogues of natural products (e.g., histidine derivatives); chemical modifications are conducted to study biological activity, commonly involving multistep organic synthesis. |
| Organic Synthesis | Construction of Specialized Heterocyclic Compounds | Leverages its specific functional group arrangement to synthesize other nitrogen-containing heterocycles—difficult to access by conventional routes—via decarboxylation, cyclization, and related reactions. |
Physical and chemical properties of 19485-38-2
Acidity coefficient |
0.66±0.10(Predicted) |
|---|---|
Boiling Point |
531.6ºC at 760mmHg |
Density |
1.63g/cm3 |
Exact Mass |
170.03300 |
Flash Point |
275.3ºC |
Melting Point |
253-254°C |
Molecular Formula |
C6H6N2O4 |
Molecular Weight |
170.12300 |
PSA |
92.42000 |
Storage condition |
Sealed in dry,Room Temperature |
Vapour Pressure |
3.92E-12mmHg at 25°C |
Spectrums of 19485-38-2
1.The NMR spectrum displayed on the page is a pre-sale reference spectrum and may differ from that of the actual received batch.
2.The accompanying documentation will include the NMR spectrum and purity analysis data for the shipped batch.
Retrosynthesis analysis of 19485-38-2
Cas:42545-22-2
Cas:19485-35-9
Q&A for CAS 19485-38-2
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Download SDS of 19485-38-2
Pictograms |
 |
|---|---|
Signal Word |
Warning |
Hazard Statements |
H302+H312+H332 Harmful if swallowed, in contact with skin or if inhaled H302 Harmful if swallowed H312 Harmful in contact with skin H315 Causes skin irritation H319 Causes serious eye irritation H332 Harmful if inhaled H335 May cause respiratory irritation |
Safety Data Sheet |
Download COA of 19485-38-2
Operate under the ISO 9001 system
