2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-dione

Base Information

Chemical Name:2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-dione
CAS No.:91680-07-8
Molecular Formula:C19H14N2O2
Molecular Weight:302.332
Hs Code.:
European Community (EC) Number:685-017-7

Synonyms:91680-07-8;2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-dione;AKOS003277828;2-benzyl-4-methyl-1H,2H,3H-pyrrolo[3,4-c]quinoline-1,3-dione

Suppliers and Price of 2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-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
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price

Total 3 raw suppliers

Chemical Property of 2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-dione

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:302.105527694
Heavy Atom Count:23
Complexity:486

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NC2=CC=CC=C2C3=C1C(=O)N(C3=O)CC4=CC=CC=C4

Technology Process of 2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-dione

There total 5 articles about 2-Benzyl-4-methyl-1H-pyrrolo[3,4-c]quinoline-1,3(2H)-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: 86.0%

: 91680-16-9
N-[2-(1-Benzyl-2,5-dioxo-pyrrolidin-3-yl)-phenyl]-thioacetimidic acid ethyl ester

: 91680-07-8
2-benzyl-4-dimethyl-1H-pyrrole[3,4-c]quinoline-1,3(2H)-dione

Guidance literature:: With lithium tert-butoxide; In dimethyl sulfoxide; tert-butyl alcohol; at 20 ℃;

Reference yield: 68.0%

: 882-36-0
N-benzyl-3-oxobutanamide

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 91680-07-8
2-benzyl-4-dimethyl-1H-pyrrole[3,4-c]quinoline-1,3(2H)-dione

Guidance literature:: With 1-butyl-3-methylimidazolium Tetrafluoroborate; In toluene; at 100 ℃; for 0.666667h; Inert atmosphere; Combinatorial reaction / High throughput screening (HTS); Microwave irradiation; Green chemistry;
DOI:10.1021/co500002s