1-Amino-3-phenylindole

Base Information

• Chemical Name: 1-Amino-3-phenylindole
• CAS No.: 3929-81-5
• Molecular Formula: C14H12N2
• Molecular Weight: 208.263
• UNII: CFT35SZK47
• DSSTox Substance ID: DTXSID60605656
• Nikkaji Number: J3.524.758K
• Wikidata: Q4545764
• Wikipedia: 1-Amino-3-phenylindole
• Mol file: 3929-81-5.mol

Synonyms:1-Amino-3-phenylindole;3-Phenyl-1H-indol-1-amine;3929-81-5;CFT35SZK47;Indole, 1-amino-3-phenyl-;1H-Indol-1-amine, 3-phenyl-;UNII-CFT35SZK47;1h-indol-1-amine,3-phenyl-;1-amino-3-phenyl-indole;SCHEMBL9366056;DTXSID60605656;SZBSSFJINJSGMH-UHFFFAOYSA-N;Q4545764

Chemical Property of 1-Amino-3-phenylindole

Chemical Property:

• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 208.100048391
• Heavy Atom Count: 16
• Complexity: 235

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CN(C3=CC=CC=C32)N

Technology Process of 1-Amino-3-phenylindole

There total 5 articles about 1-Amino-3-phenylindole 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: 38.0%

3-phenyl-1H-indole (1504-16-1) → 1-amino-3-phenylindole (3929-81-5)

Guidance literature:

With potassium hydroxide; hydroxylamine-O-sulfonic acid; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 24h; Inert atmosphere;

DOI:10.1002/chem.201503927

Reference yield:

4-(N,N'-bis-ethoxycarbonyl-hydrazino)-4-phenyl-3,4-dihydro-cinnoline-1,2-dicarboxylic acid diethyl ester → 1-amino-3-phenylindole (3929-81-5)

Guidance literature:

With hydrazine hydrate; at 180 ℃;

Reference yield:

1-nitroso-3-phenyl-indole → 1-amino-3-phenylindole (3929-81-5)

Guidance literature:

With diethyl ether; platinum; Hydrogenation;

upstream raw materials:

1-acetyl-amino-3-phenylindole

3-phenyl-1H-indole

Downstream raw materials:

1-acetyl-amino-3-phenylindole

benzylidene-(3-phenyl-indol-1-yl)-amine

3-phenyl-1H-indole

1-(3'-bromopropionylamino)-3-phenyl-indole

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