1-Phenyl-2,3-dihydro-1H-indole

Base Information

Chemical Name:1-Phenyl-2,3-dihydro-1H-indole
CAS No.:25083-11-8
Molecular Formula:C14H13N
Molecular Weight:195.264
Hs Code.:2933990090
DSSTox Substance ID:DTXSID20432182
Nikkaji Number:J1.069.364K
Wikidata:Q82246237
Mol file:25083-11-8.mol

Synonyms:1-phenylindoline;1-PHENYL-2,3-DIHYDRO-1H-INDOLE;25083-11-8;phenylindoline;SCHEMBL3905172;DTXSID20432182;AKOS006331305

Suppliers and Price of 1-Phenyl-2,3-dihydro-1H-indole

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
1-PHENYL-2,3-DIHYDRO-1H-INDOLE 95.00%
5MG
$ 499.09

Total 6 raw suppliers

Chemical Property of 1-Phenyl-2,3-dihydro-1H-indole

Chemical Property:

PSA：3.24000
LogP:3.44580
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:195.104799419
Heavy Atom Count:15
Complexity:207

Purity/Quality:

99% ^*data from raw suppliers

1-PHENYL-2,3-DIHYDRO-1H-INDOLE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(C2=CC=CC=C21)C3=CC=CC=C3

Technology Process of 1-Phenyl-2,3-dihydro-1H-indole

There total 19 articles about 1-Phenyl-2,3-dihydro-1H-indole 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: 99.0%

: 496-15-1
1-indoline

: 108-90-7
chlorobenzene

: 25083-11-8
N-Phenyl-2,3-dihydroindole

Guidance literature:: With dicyclohexyl(4''-methoxy-[1,1':2',1''-terphenyl]-2-yl)phosphine; bis(dibenzylideneacetone)-palladium⁽⁰⁾; sodium t-butanolate; In tert-butyl alcohol; at 110 ℃; for 18h; Inert atmosphere; Schlenk technique;
DOI:10.1002/adsc.202100283

Reference yield: 97.0%

: 496-15-1
1-indoline

: 88284-48-4
2-(trimethylsilyl)phenyl trifluoromethanesulfonate

: 25083-11-8
N-Phenyl-2,3-dihydroindole

Guidance literature:: With cesium fluoride; In acetonitrile; at 20 ℃; for 5h;
DOI:10.1021/jo0602221

Reference yield: 92.0%

: 496-15-1
1-indoline

: 108-86-1,52753-63-6
bromobenzene

: 25083-11-8
N-Phenyl-2,3-dihydroindole

Guidance literature:: With dicyclohexyl(2-methoxy-6-methylbiphenyl-2^,-yl)phosphine; potassium tert-butylate; palladium diacetate; In 1,4-dioxane; at 160 ℃; for 0.166667h; Microwave irradiation; Inert atmosphere;
DOI:10.1002/ejoc.201500962