1-(Prop-2-yn-1-yl)indolin-2-one

Base Information

Chemical Name:1-(Prop-2-yn-1-yl)indolin-2-one
CAS No.:37994-11-9
Molecular Formula:C11H9NO
Molecular Weight:171.199
Hs Code.:
DSSTox Substance ID:DTXSID10433709
Wikidata:Q82247919
Mol file:37994-11-9.mol

Synonyms:1-(Prop-2-yn-1-yl)indolin-2-one;37994-11-9;1-prop-2-ynyl-3H-indol-2-one;2H-Indol-2-one, 1,3-dihydro-1-(2-propynyl)-;SCHEMBL5661000;DTXSID10433709;SB65792;CS-0094836;D75632;A912859

Suppliers and Price of 1-(Prop-2-yn-1-yl)indolin-2-one

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

Total 6 raw suppliers

Chemical Property of 1-(Prop-2-yn-1-yl)indolin-2-one

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:171.068413911
Heavy Atom Count:13
Complexity:263

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C#CCN1C(=O)CC2=CC=CC=C21

Technology Process of 1-(Prop-2-yn-1-yl)indolin-2-one

There total 1 articles about 1-(Prop-2-yn-1-yl)indolin-2-one 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: 1.2%

: 59-48-3
2-oxoindole

: 106-96-7
propargyl bromide

: 37994-11-9
1-Prop-2-ynyl-1,3-dihydroindol-2-one

: 112476-59-2
3,3-Dipropinylindolin-2-on

: 112476-58-1
1,3,3-Tripropinylindolin-2-on

: prop-2-yn-1-yl 2-(prop-2-yn-1-ylamino)benzoate

Guidance literature:: With sodium hydroxide; potassium iodide; tetrabutyl-ammonium chloride; In toluene; at 50 ℃; for 72h;
DOI:10.1002/ardp.19873200812

Reference yield: 83.0%

: 37994-11-9
1-Prop-2-ynyl-1,3-dihydroindol-2-one

: 4260-34-8
3-benzyl-2-methyl-3H-quinazolin-4-one

: (E)-3-benzyl-2-((2-oxo-1-(prop-2-yn-1-yl)indolin-3-ylidene)methyl)quinazolin-4(3H)-one

Guidance literature:: With iron(II) acetate; In N,N-dimethyl-formamide; at 120 ℃; for 4h;
DOI:10.1016/j.tetlet.2021.153141

Reference yield: 50.0%

: 67860-41-7
4-(2-chlorophenyl)2-iodo-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine

: 37994-11-9
1-Prop-2-ynyl-1,3-dihydroindol-2-one

: 125030-40-2
1-[3-[4-(2-Chlorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo [-4,3-a][1,4]diazepin-2-yl]-2-propynyl]-1,3-dihydro2H-indol-2-one

Guidance literature:: With copper(l) iodide; palladium diacetate; triethylamine; triphenylphosphine; In N,N-dimethyl-formamide; for 72h; Ambient temperature;
DOI:10.1021/jm00107a048