Nb-acetyl-2-indolylmethanamine

Base Information

Chemical Name:Nb-acetyl-2-indolylmethanamine
CAS No.:1392446-61-5
Molecular Formula:C₁₁H₁₂N₂O
Molecular Weight:188.229
Hs Code.:

Synonyms:Nb-acetyl-2-indolylmethanamine

Suppliers and Price of Nb-acetyl-2-indolylmethanamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of Nb-acetyl-2-indolylmethanamine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of Nb-acetyl-2-indolylmethanamine

There total 2 articles about Nb-acetyl-2-indolylmethanamine 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: 75.0%

: 21109-25-1
1-(1H-indol-2-yl)methanamine

: 108-24-7
acetic anhydride

: 1392446-61-5
Nb-acetyl-2-indolylmethanamine

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jf302038a

Reference yield:

: 21109-25-1
1-(1H-indol-2-yl)methanamine

: 1392446-61-5
Nb-acetyl-2-indolylmethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; triethylamine

2: Leptosphaeria maculans / acetonitrile / 48 h / Enzymatic reaction

With pyridine; triethylamine; In acetonitrile;
DOI:10.1021/jf302038a

Reference yield: 39.0%

: 1392446-61-5
Nb-acetyl-2-indolylmethanamine

: 94011-49-1
diethyl phenacylmalonate

: C₂₆H₂₆N₂O₆

Guidance literature:: With copper diacetate; potassium carbonate; In dimethyl sulfoxide; at 100 ℃; for 4h; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.joc.0c00624