1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione

Base Information

• Chemical Name: 1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione
• CAS No.: 33693-09-3
• Molecular Formula: C15H13NS
• Molecular Weight: 239.341
• DSSTox Substance ID: DTXSID001240435
• Nikkaji Number: J1.500.076G

Synonyms:DTXSID001240435;33693-09-3;1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione

Chemical Property of 1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione

Chemical Property:

• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 239.07687059
• Heavy Atom Count: 17
• Complexity: 295

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CN1C2=CC=CC=C2C(C1=S)C3=CC=CC=C3

Technology Process of 1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione

There total 2 articles about 1,3-Dihydro-1-methyl-3-phenyl-2H-indole-2-thione 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:

phenyl-thioacetic acid-(N'-methyl-N'-phenyl-hydrazide) (69677-51-6) → 1-methyl-3-phenyl-1,3-dihydro-indole-2-thione (33693-09-3)

Guidance literature:

With hydrogenchloride; methanol;

Reference yield:

→ 1-methyl-3-phenyl-1,3-dihydro-indole-2-thione (33693-09-3)

Guidance literature:

DOI:10.1039/C29710000836

Reference yield: 99.0%

1-methyl-3-phenyl-1,3-dihydro-indole-2-thione (33693-09-3) + allyl bromide (106-95-6) → 1-methyl-2-allylthio-3-phenylindole

Guidance literature:

With potassium carbonate; In acetone; for 0.5h; Ambient temperature;

upstream raw materials:

phenyl-thioacetic acid-(N'-methyl-N'-phenyl-hydrazide)

Downstream raw materials:

N-methyl-3-phenylindole

bis(1-methyl-3-phenylindol-2-yl) sulfide

2-ethoxycarbonylmethylthio-N-methyl-3-phenylindole

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