N-benzyl-1H-indole-3-carboxamide

Base Information

Chemical Name:N-benzyl-1H-indole-3-carboxamide
CAS No.:61788-25-8
Molecular Formula:C16H14N2O
Molecular Weight:250.3
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50363233
Nikkaji Number:J3.488.220G
Wikidata:Q82146833
Mol file:61788-25-8.mol

Synonyms:N-benzyl-1H-indole-3-carboxamide;61788-25-8;1H-INDOLE-3-CARBOXYLIC ACID BENZYLAMIDE;SCHEMBL8251765;DTXSID50363233;MFCD03305733;AKOS008967468;6T-1487

Suppliers and Price of N-benzyl-1H-indole-3-carboxamide

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
Packaging
price

American Custom Chemicals Corporation
N-BENZYL-1H-INDOLE-3-CARBOXAMIDE 95.00%
10MG
$ 675.51

American Custom Chemicals Corporation
N-BENZYL-1H-INDOLE-3-CARBOXAMIDE 95.00%
5MG
$ 667.02

American Custom Chemicals Corporation
N-BENZYL-1H-INDOLE-3-CARBOXAMIDE 95.00%
1MG
$ 628.20

Total 2 raw suppliers

Chemical Property of N-benzyl-1H-indole-3-carboxamide

Chemical Property:

PSA：48.38000
LogP:3.67270
XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:250.110613074
Heavy Atom Count:19
Complexity:312

Purity/Quality:

98% ^*data from raw suppliers

N-BENZYL-1H-INDOLE-3-CARBOXAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=O)C2=CNC3=CC=CC=C32

Technology Process of N-benzyl-1H-indole-3-carboxamide

There total 7 articles about N-benzyl-1H-indole-3-carboxamide 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: 78.0%

: 19194-62-8
1H-indol-3-yl(oxo)acetonitrile

: 100-46-9
benzylamine

: 61788-25-8
N-phenylmethyl-1H-indolyl-3-carboxamide

Guidance literature:: In acetonitrile; for 6h; Reflux;
DOI:10.1016/j.tetlet.2015.02.090

Reference yield: 73.0%

indole-3-carbinol: 700-06-1
indole-3-carbinol

: 100-46-9
benzylamine

: 61788-25-8
N-phenylmethyl-1H-indolyl-3-carboxamide

Guidance literature:: With [Ru(Cl)(CO)(κ2-S,NN-N-(4-methylphenyl)pyridine-2-thiocarboxamide)(AsPh3)2]; In tert-butyl alcohol; at 62 ℃; for 8h;
DOI:10.1021/om500556b

Reference yield:

: 771-50-6
1H-indole-3-carboxylic acid

: 100-46-9
benzylamine

: 61788-25-8
N-phenylmethyl-1H-indolyl-3-carboxamide

Guidance literature:: With 1-Methylpyrrolidine; diphenylsilane; In acetonitrile; at 100 ℃; for 1h; Microwave irradiation; Green chemistry;
DOI:10.1039/d0gc02833a