3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one

Base Information

Chemical Name:3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one
CAS No.:1025736-33-7
Molecular Formula:C₁₅H₁₄N₂O
Molecular Weight:238.289
Hs Code.:
DSSTox Substance ID:DTXSID201225291
Nikkaji Number:J3.660.680K

Synonyms:1025736-33-7;3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one;3-amino-1-benzyl-3H-indol-2-one;3-amino-1-benzyl-2,3-dihydro-1H-indol-2-one;3-Amino-1-benzyl-1,3-dihydro-indol-2-one;3-amino-1-benzylindolin-2-one;DTXSID201225291;AKOS005590199;VS-10310;3-Amino-1,3-dihydro-1-(phenylmethyl)-2H-indol-2-one

Suppliers and Price of 3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of 3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:238.110613074
Heavy Atom Count:18
Complexity:312

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C3=CC=CC=C3C(C2=O)N

Technology Process of 3-amino-1-benzyl-1,3-dihydro-2H-indol-2-one

There total 3 articles about 3-amino-1-benzyl-1,3-dihydro-2H-indol-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:

: 28150-91-6
1-benzyl-3-(hydroxyimino)indolin-2-one

: 1025736-33-7
C₁₅H₁₄N₂O

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 10h; under 760.051 Torr;
DOI:10.1021/ol200724q

Reference yield:

: C₁₆H₁₄N₂O₂

: 1025736-33-7
C₁₅H₁₄N₂O

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In acetonitrile; at 20 ℃; for 6h; under 760.051 Torr;
DOI:10.1039/c9cc07346a

Reference yield:

: 1217-89-6
1-benzylisatin

: 1025736-33-7
C₁₅H₁₄N₂O

Guidance literature:: Multi-step reaction with 2 steps

1: dipotassium hydrogenphosphate / methanol / 2 h / 20 °C

2: 5%-palladium/activated carbon; hydrogen / acetonitrile / 6 h / 20 °C / 760.05 Torr

With dipotassium hydrogenphosphate; 5%-palladium/activated carbon; hydrogen; In methanol; acetonitrile;
DOI:10.1039/c9cc07346a