2-Benzoyl-1-methyl-1H-indol-3-yl acetate

Base Information

Chemical Name:2-Benzoyl-1-methyl-1H-indol-3-yl acetate
CAS No.:53278-22-1
Molecular Formula:C₁₈H₁₅NO₃
Molecular Weight:293.322
Hs Code.:
DSSTox Substance ID:DTXSID10525411
Wikidata:Q82392987
Mol file:53278-22-1.mol

Synonyms:53278-22-1;2-Benzoyl-1-methyl-1H-indol-3-yl acetate;DTXSID10525411

Suppliers and Price of 2-Benzoyl-1-methyl-1H-indol-3-yl acetate

Supply Marketing:

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

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Chemical Property of 2-Benzoyl-1-methyl-1H-indol-3-yl acetate

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:293.10519334
Heavy Atom Count:22
Complexity:430

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)OC1=C(N(C2=CC=CC=C21)C)C(=O)C3=CC=CC=C3

Technology Process of 2-Benzoyl-1-methyl-1H-indol-3-yl acetate

There total 3 articles about 2-Benzoyl-1-methyl-1H-indol-3-yl acetate 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: 13.0%

: 1025-99-6
(1-methyl-1H-indol-2-yl)(phenyl)methanone

: 53278-22-1
(3-acetoxy-1-methyl-indol-2-yl)-phenyl-methanone

Guidance literature:: With lead(IV) acetate; In dichloromethane; for 22h; Heating;

Reference yield:

: 1022-86-2
2-benzoylindole

: 53278-22-1
(3-acetoxy-1-methyl-indol-2-yl)-phenyl-methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) DMSO, 1 h

2: 13 percent / lead tetra-acetate / CH₂Cl₂ / 22 h / Heating

With lead(IV) acetate; sodium hydride; In dichloromethane;