Indole-3-carboxylic acid
98%
- Product Code: 122451
Alias:
Indole-3-carboxylic acid ; 3-Indolecarboxylic acid
CAS:
771-50-6
| Molecular Weight: | 161.16 g./mol | Molecular Formula: | C₉H₇NO₂ |
|---|---|---|---|
| EC Number: | 212-231-6 | MDL Number: | MFCD00005624 |
| Melting Point: | 232-234 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Indole-3-carboxylic acid is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, including potential drugs targeting neurological disorders and cancer. Its structure is valuable in the development of indole-based molecules, which are known for their diverse biological activities. Additionally, it is utilized in the study of plant growth regulators and as a building block in the synthesis of agrochemicals. Its role in research extends to investigating enzyme interactions and metabolic pathways, particularly those involving indole derivatives.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Purity (T) | 97.5-102.5 |
| Appearance | White To Pale Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $13.56 |
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| 5.000 | 10-20 days | $14.57 |
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| 25.000 | 10-20 days | $35.66 |
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| 100.000 | 10-20 days | $104.97 |
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| 500.000 | 10-20 days | $469.61 |
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Indole-3-carboxylic acid
Indole-3-carboxylic acid is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, including potential drugs targeting neurological disorders and cancer. Its structure is valuable in the development of indole-based molecules, which are known for their diverse biological activities. Additionally, it is utilized in the study of plant growth regulators and as a building block in the synthesis of agrochemicals. Its role in research extends to investigating enzyme interactions and metabolic pathways, particularly those involving indole derivatives.
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