| Identification | More | [Name]
5-Methoxyindole-3-acetic acid | [CAS]
3471-31-6 | [Synonyms]
5-METHOXY-3-INDOLEACETIC ACID
5-METHOXYINDOLE-3-ACETIC ACID
RARECHEM AL BO 1466
TIMTEC-BB SBB003497
5-methoxy-indole-3-aceticaci
5-methoxyindoleaceticacid
5-methoxyindol-3-ylacetic acid
5-Methoxy-3-indolaceticacid
5-Methoxyindole-3-aceticacid,98+%
5-METHOXYINDOLE-3-ACETIC ACID ABOUT 99%
5-MeO-IAA
5-Methoxy-1H-indole-3-acetic acid
5-Methoxy-3-indolylacetic acid
5-Methoxy-IAA
5-Mehtoxyindoleacetic acid | [EINECS(EC#)]
222-438-3 | [Molecular Formula]
C11H11NO3 | [MDL Number]
MFCD00005638 | [Molecular Weight]
205.21 | [MOL File]
3471-31-6.mol |
| Chemical Properties | Back Directory | [Appearance]
OFF-WHITE TO SLIGHTLY BEIGE CRYSTALLINE POWDER | [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. ]
2-8°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 Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
NL3660500
| [HS Code ]
29339900 |
| Hazard Information | Back Directory | [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]
5-Methoxyindole-3-acetic Acid is a chemical reagent used in the analysis of the physiological properties of auxins. | [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. | [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. |
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