N-phenyl-2,3-dihydro-1H-indole-1-carboxamide

Base Information

Chemical Name:N-phenyl-2,3-dihydro-1H-indole-1-carboxamide
CAS No.:61589-28-4
Molecular Formula:C15H14N2O
Molecular Weight:238.289
Hs Code.:
DSSTox Substance ID:DTXSID10353635
Wikidata:Q82131343
ChEMBL ID:CHEMBL1571426

Synonyms:N-phenyl-2,3-dihydro-1H-indole-1-carboxamide;MLS000121635;61589-28-4;N-phenyl-1-indolinecarboxamide;1H-Indole-1-carboxamide, 2,3-dihydro-N-phenyl-;2,3-Dihydro-indole-1-carboxylic acid phenylamide;SMR000119057;N-phenyl-2,3-dihydroindole-1-carboxamide;Oprea1_360824;Oprea1_497071;SCHEMBL382910;N-phenylindoline-1-carboxamide;cid_746892;CHEMBL1571426;BDBM49359;DTXSID10353635;HMS1683E14;HMS2379D10;STK017709;AKOS000633380;SR-01000493471;SR-01000493471-1

Suppliers and Price of N-phenyl-2,3-dihydro-1H-indole-1-carboxamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-phenyl-2,3-dihydro-1H-indole-1-carboxamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:238.110613074
Heavy Atom Count:18
Complexity:299

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(C2=CC=CC=C21)C(=O)NC3=CC=CC=C3

Technology Process of N-phenyl-2,3-dihydro-1H-indole-1-carboxamide

There total 2 articles about N-phenyl-2,3-dihydro-1H-indole-1-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: 70.0%

: 496-15-1
1-indoline

: 2040-76-8
phenylcarbamic acid chloride

: 61589-28-4
N-phenylindoline-1-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 3.25h;
DOI:10.1021/jo502733q

Reference yield: 58.0%

: 496-15-1
1-indoline

: N-fluoro-N-(phenylsulfonyl)benzamide

: 61589-28-4
N-phenylindoline-1-carboxamide

Guidance literature:: With dmap; potassium carbonate; In tetrahydrofuran; at 50 ℃; for 12h;
DOI:10.1002/ejoc.201901602

Reference yield: 67.0%

: 61589-28-4
N-phenylindoline-1-carboxamide

: 19226-36-9
3-phenyl-5H-1,4,2-dioxazol-5-one

: 7-benzamido-N-phenylindoline-1-carboxamide

Guidance literature:: With silver hexafluoroantimonate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; Trimethylacetic acid; In 2,2,2-trifluoroethanol; for 24h;
DOI:10.1021/acs.joc.7b02500