5-methoxy-4-methyl-1H-indole

Base Information

• Chemical Name: 5-methoxy-4-methyl-1H-indole
• CAS No.: 302912-21-6
• Molecular Formula: C₁₀H₁₁NO
• Molecular Weight: 161.203
• Hs Code.: 2933990090
• European Community (EC) Number: 623-623-5
• DSSTox Substance ID: DTXSID30391175
• Nikkaji Number: J1.760.570D
• Wikidata: Q82188446
• Mol file: 302912-21-6.mol

Synonyms:5-methoxy-4-methyl-1H-indole;302912-21-6;5-Methoxy-4-methylindole;1H-Indole, 5-methoxy-4-methyl-;5-methoxy-4-methyl-indole;SCHEMBL1400405;4-Methyl-5-methoxy-1H-indole;DTXSID30391175;5-Methoxy-4-methylindole, 98%;RISMXZVKSIWLMK-UHFFFAOYSA-N;AS-60252;A12401;M-3532;A820299;InChI=1/C10H11NO/c1-7-8-5-6-11-9(8)3-4-10(7)12-2/h3-6,11H,1-2H

Chemical Property of 5-methoxy-4-methyl-1H-indole

Chemical Property:

• Melting Point: 76-79 °C(lit.)
• PSA: 25.02000
• LogP: 2.48490
• Storage Temp.: 2-8°C
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 161.084063974
• Heavy Atom Count: 12
• Complexity: 160

Purity/Quality:

97% ^*data from raw suppliers

5-Methoxy-4-methylindole 98% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=C(C=CC2=C1C=CN2)OC
• Uses: Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2. Reactant for preparation of indolyl and isoquinolinyl anthranilates as PPARδ partial agonists 2 Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2Reactant for preparation of indolyl and isoquinolinyl anthranilates as PPARδ partial agonists

Technology Process of 5-methoxy-4-methyl-1H-indole

There total 1 articles about 5-methoxy-4-methyl-1H-indole 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:

1-[2-(3-methoxy-2-methyl-6-nitrophenyl)-vinyl]-pyrrolidine (879093-18-2) → 5-methoxy-4-methyl-1H-indole (302912-21-6)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethyl acetate; at 20 ℃; for 3h; under 2585.81 Torr;

Reference yield:

C15H11Cl2NO5S (1066821-85-9) + 5-methoxy-4-methyl-1H-indole (302912-21-6) → C25H21ClN2O6S

Guidance literature:

With 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine; In acetonitrile; at 20 ℃;

DOI:10.1016/j.bmcl.2008.08.011

Reference yield:

C16H14ClNO5S (1066822-02-3) + 5-methoxy-4-methyl-1H-indole (302912-21-6) → C26H24N2O6S

Guidance literature:

With 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine; In acetonitrile; at 20 ℃;

DOI:10.1016/j.bmcl.2008.08.011

upstream raw materials:

1-[2-(3-methoxy-2-methyl-6-nitrophenyl)-vinyl]-pyrrolidine

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