N-benzyl-2-(1H-indol-3-yl)acetamide

Base Information

Chemical Name:N-benzyl-2-(1H-indol-3-yl)acetamide
CAS No.:73031-14-8
Molecular Formula:C₁₇H₁₆N₂O
Molecular Weight:264.327
Hs Code.:
European Community (EC) Number:684-773-5
Nikkaji Number:J983.659D

Synonyms:N-benzyl-2-(1H-indol-3-yl)acetamide;73031-14-8;ChemDiv3_004400;Oprea1_118695;Oprea1_692998;F1108-0022;SCHEMBL1853622;HMS1485H22;AKOS001119541;IDI1_022310;CS-0295171;EU-0014578;BRD-K99733125-001-01-1;Z27749578

Suppliers and Price of N-benzyl-2-(1H-indol-3-yl)acetamide

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 N-benzyl-2-(1H-indol-3-yl)acetamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:264.126263138
Heavy Atom Count:20
Complexity:325

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=O)CC2=CNC3=CC=CC=C32

Technology Process of N-benzyl-2-(1H-indol-3-yl)acetamide

There total 10 articles about N-benzyl-2-(1H-indol-3-yl)acetamide 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: 98.0%

: 143-07-7
lauric acid

: 100-46-9
benzylamine

: 73031-14-8
2-(1H-indol-3-yl)-N-benzyl acetamide

: 67264-80-6
N-benzyl-3,3-dimethylacrylic amide

: 78172-96-0
benzamide of lauric acid

Guidance literature:: With potassium hydroxide; bis(o-nitrophenyl)phenylphosphonate; 4 A molecular sieve; tetrabutylammomium bromide; other acids; multistep reaction;
DOI:10.1246/cl.1981.285

Reference yield: 91.0%

: 87-51-4
indole-3-acetic acid

: 100-46-9
benzylamine

: 73031-14-8
2-(1H-indol-3-yl)-N-benzyl acetamide

Guidance literature:: With sulphate-modified mesoporous carbon; In toluene; at 110 ℃; for 10h;
DOI:10.1166/jnn.2018.14563

Reference yield: 85.0%

: 73031-14-8
2-(1H-indol-3-yl)-N-benzyl acetamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 16h;