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| 5-Methoxyindole-3-acetic acid Basic information |
| 5-Methoxyindole-3-acetic acid Chemical Properties |
Melting point | 145-148 °C (dec.)(lit.) | Boiling point | 343.88°C (rough estimate) | density | 1.2235 (rough estimate) | refractive index | 1.5130 (estimate) | storage temp. | Keep in dark place,Sealed in dry,Store in freezer, under -20°C | solubility | DMSO (Slightly), Methanol (Slightly) | form | crystalline | pka | 4.52±0.30(Predicted) | color | light yellow to tan | Water Solubility | insoluble | BRN | 187161 | CAS DataBase Reference | 3471-31-6(CAS DataBase Reference) |
Safety Statements | 24/25 | WGK Germany | 3 | RTECS | NL3660500 | HS Code | 29339900 |
| 5-Methoxyindole-3-acetic acid Usage And Synthesis |
Chemical Properties | OFF-WHITE TO SLIGHTLY BEIGE CRYSTALLINE POWDER | Uses | - Reactant for preparation of aryloxybenzothiazoles as inhibitors of NO production
- Reactant for preparation of transcription inhibitors of novel Gli1 as antitumor agents
- Reactant for preparation of indole derivatives as NR2B/NMDA receptor antagonists
- Reactant for preparation of indolyl esters and amides related to indomethacin as selective COX-2 inhibitors
- Reactant for preparation of quinoline salicylic acid series of P-selectin antagonists
- Reactant for preparation of prostaglandin D2 receptor antagonists
| Uses | Reactant for preparation of aryloxybenzothiazoles as inhibitors of NO production 1 Reactant for preparation of transcription inhibitors of novel Gli1 as antitumor agents Reactant for preparation of indole derivatives as NR2B/NMDA receptor antagonists 2 Reactant for preparation of indolyl esters and amides related to indomethacin as selective COX-2 inhibitors 3 Reactant for preparation of quinoline salicylic acid series of P-selectin antagonists 4 Reactant for preparation of prostaglandin D2 receptor antagonists. | Uses | 5-Methoxyindole-3-acetic Acid is a chemical reagent used in the analysis of the physiological properties of auxins. | Definition | ChEBI: 5-methoxyindole-3-acetic acid is a member of the class of indole-3-acetic acids in which the hydrogen at position 5 of indole-3-acetic acid has been replaced by a methoxy group. It has a role as a Brassica napus metabolite, a human urinary metabolite, an antibacterial agent, a marine xenobiotic metabolite, a carcinogenic agent and a rat metabolite. It is a member of indole-3-acetic acids and an aromatic ether. |
| 5-Methoxyindole-3-acetic acid Preparation Products And Raw materials |
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