5-Methoxyindole-3-acetic acid

5-Methoxyindole-3-acetic acid Basic information
Product Name:5-Methoxyindole-3-acetic acid
Synonyms:2-(5-Methoxy-3-indolyl)acetic acid;5-Methoxy-3-indoleacetic acid 98%;5-methoxy-indole-3-aceticaci;5-methoxyindoleaceticacid;RARECHEM AL BO 1466;TIMTEC-BB SBB003497;5-METHOXYINDOLE-3-ACETIC ACID;5-METHOXY-3-INDOLEACETIC ACID
CAS:3471-31-6
MF:C11H11NO3
MW:205.21
EINECS:222-438-3
Product Categories:Indoline & Oxindole;Indoles and derivatives;Heterocyclic Compounds;Indoles;Simple Indoles;Building Blocks;Heterocyclic Building Blocks
Mol File:3471-31-6.mol
5-Methoxyindole-3-acetic acid Structure
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)
pka4.52±0.30(Predicted)
form crystalline
color light yellow to tan
Water Solubility insoluble
BRN 187161
CAS DataBase Reference3471-31-6(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
RTECS NL3660500
HS Code 29339900
MSDS Information
ProviderLanguage
5-Methoxyindole-3-acetic acid English
ACROS English
SigmaAldrich English
ALFA English
5-Methoxyindole-3-acetic acid Usage And Synthesis
Chemical PropertiesOFF-WHITE TO SLIGHTLY BEIGE CRYSTALLINE POWDER
UsesReactant 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.
Uses5-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
  • 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
DefinitionChEBI: 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
Indorenate niometacin CP 331 Acemetacin 1-(p-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-acetic acid zidometacin 1-(P-CHLORBENZOYL)-5-METHOXY-2-METHYL INDOLE-3-ACETIC ACID [2-14C]- indomethacin triethylene ester 5-METHOXY-2-METHYL-3-INDOLEACETIC ACID cinmetacin 1-(2-Cyclohexyl-2-oxoethyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid 5-BENZYLOXYINDOLE-3-ACETIC ACID INDOMETHACIN SODIUM SALT TRIHYDRATE 5-Methoxyindole-3-acetic acid AURORA KA-4884 Talmetacin PROGLUMETACIN MALEATE TROPESIN

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.