5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid

Base Information

• Chemical Name: 5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid
• CAS No.: 105909-93-1
• Molecular Formula: C₁₂H₁₃NO₃
• Molecular Weight: 219.24
• Hs Code.: 2933990090
• European Community (EC) Number: 866-273-0
• DSSTox Substance ID: DTXSID20351723
• Nikkaji Number: J1.076.626E
• Wikidata: Q82128355
• Mol file: 105909-93-1.mol

Synonyms:5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid;105909-93-1;5-methoxy-1,2-dimethylindole-3-carboxylic acid;MFCD00458840;5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylicacid;ChemDiv2_004332;Cambridge id 5258918;Oprea1_009087;Oprea1_247162;CBDivE_015851;SCHEMBL3384928;DTXSID20351723;HMS1381E20;BBL028624;STL360350;AKOS000588859;CCG-114440;IDI1_003047;VS-08877;CS-0055917;EU-0081512;FT-0704619;D86122;EN300-261564;AB00077149-01;Z57396004;5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid, AldrichCPR

Chemical Property of 5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid

Chemical Property:

• Vapor Pressure: 4.65E-08mmHg at 25°C
• Boiling Point: 427.2°C at 760 mmHg
• Flash Point: 212.2°C
• PSA: 51.46000
• Density: 1.23g/cm³
• LogP: 2.19350
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 219.08954328
• Heavy Atom Count: 16
• Complexity: 281

Purity/Quality:

97% ^*data from raw suppliers

5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi,T
• Statements: 25
• Safety Statements: 45

MSDS Files:

Useful:

• Canonical SMILES: CC1=C(C2=C(N1C)C=CC(=C2)OC)C(=O)O

Technology Process of 5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid

There total 3 articles about 5-Methoxy-1,2-dimethyl-1H-indole-3-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethyl 5-methoxy-1,2-dimethyl-1H-indole-3-carboxylate (40963-98-2) → 5-methoxy-1,2-dimethyl-indole-3-carboxylic acid (105909-93-1)

Guidance literature:

With potassium hydroxide;

Reference yield:

mecarbinate (15574-49-9) → 5-methoxy-1,2-dimethyl-indole-3-carboxylic acid (105909-93-1)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous NaOH; dioxane

2: ethanolic KOH

With 1,4-dioxane; potassium hydroxide; sodium hydroxide;

Reference yield:

→ 5-methoxy-1,2-dimethyl-indole-3-carboxylic acid (105909-93-1)

Guidance literature:

upstream raw materials:

ethyl 5-methoxy-1,2-dimethyl-1H-indole-3-carboxylate

mecarbinate