1-Benzyl-5-methoxyindoline-2,3-dione

Base Information

Chemical Name:1-Benzyl-5-methoxyindoline-2,3-dione
CAS No.:16077-10-4
Molecular Formula:C16H13NO3
Molecular Weight:267.284
Hs Code.:
DSSTox Substance ID:DTXSID70463481
Nikkaji Number:J1.358.493A
Wikidata:Q82288373
Mol file:16077-10-4.mol

Synonyms:16077-10-4;1-benzyl-5-methoxyindoline-2,3-dione;1-BENZYL-5-METHOXY-2,3-DIHYDRO-1H-INDOLE-2,3-DIONE;N-Benzyl-5-methoxyisatin;1H-Indole-2,3-dione, 5-methoxy-1-(phenylmethyl)-;1-BENZYL-5-METHOXYINDOLE-2,3-DIONE;SCHEMBL578232;DTXSID70463481;ZBLQKVFGHHQVMS-UHFFFAOYSA-N;MFCD18264347;AKOS010611748;SB65821;AS-67773;CS-0320863;W13001

Suppliers and Price of 1-Benzyl-5-methoxyindoline-2,3-dione

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

Crysdot
1-Benzyl-5-methoxyindoline-2,3-dione 97%
1g
$ 656.00

Crysdot
1-Benzyl-5-methoxyindoline-2,3-dione 97%
5g
$ 1975.00

Chemenu
1-Benzyl-5-methoxyindoline-2,3-dione 95%+
5g
$ 1861.00

Chemenu
1-Benzyl-5-methoxyindoline-2,3-dione 95%+
1g
$ 620.00

aablocks
1-Benzyl-5-methoxy-2,3-dihydro-1h-indole-2,3-dione 95%
1g
$ 471.00

Total 6 raw suppliers

Chemical Property of 1-Benzyl-5-methoxyindoline-2,3-dione

Chemical Property:

PSA：46.61000
LogP:2.48970
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:267.08954328
Heavy Atom Count:20
Complexity:389

Purity/Quality:

99% ^*data from raw suppliers

1-Benzyl-5-methoxyindoline-2,3-dione 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)N(C(=O)C2=O)CC3=CC=CC=C3

Technology Process of 1-Benzyl-5-methoxyindoline-2,3-dione

There total 10 articles about 1-Benzyl-5-methoxyindoline-2,3-dione 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: 96.0%

: 39755-95-8
5-methoxyisatine

: 100-39-0
benzyl bromide

: 16077-10-4
N-benzyl-5-methoxyisatin

Guidance literature:: With sodium hydride; In DMF (N,N-dimethyl-formamide); at 0 ℃; for 1h;

Reference yield: 90.0%

: 39755-95-8
5-methoxyisatine

: 16077-10-4
N-benzyl-5-methoxyisatin

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.8b01827

Reference yield: 80.0%

: benzyl(4-methoxy-2-vinylphenyl)amine

: 16077-10-4
N-benzyl-5-methoxyisatin

Guidance literature:: With iodine; oxygen; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dimethyl sulfoxide; at 20 - 100 ℃; for 13h;
DOI:10.1021/acs.joc.5b00581