5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-one

Base Information

Chemical Name:5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-one
CAS No.:52817-91-1
Molecular Formula:C17H13N3O
Molecular Weight:275.31
Hs Code.:
DSSTox Substance ID:DTXSID70492478
Wikidata:Q82338409

Synonyms:52817-91-1;5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-one;DTXSID70492478;5-Methyl-1-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indol-4-one

Suppliers and Price of 5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-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 5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-one

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:275.105862047
Heavy Atom Count:21
Complexity:455

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CC=CC=C2C3=C1C(=O)NN=C3C4=CC=CC=C4

Technology Process of 5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-one

There total 6 articles about 5-Methyl-1-phenyl-3H-pyridazino[4,5-b]indol-4(5H)-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: 98.0%

: 51916-89-3
5-methyl-1-phenyl-1,2,3,5-tetrahydro-pyrazino[4,5-b]indol-4-one

: 52817-91-1
3,4-dihydro-5-methyl-4-oxo-1-phenyl-5H-pyridazino<4,5-b>indole

Guidance literature:: With potassium permanganate; In chloroform; for 6h; Ambient temperature;

Reference yield:

: 51917-14-7
1-Methyl-1H-indole-2-carboxylic acid [1-phenyl-meth-(E)-ylidene]-hydrazide

: 52817-91-1
3,4-dihydro-5-methyl-4-oxo-1-phenyl-5H-pyridazino<4,5-b>indole

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / CHCl₃ / Heating

2: conc. HCl / ethanol / 6 h / Heating

3: 80percent N₂H₄*H₂O / 6 h / Heating

4: 98 percent / 0.1 M KMnO₄ / CHCl₃ / 6 h / Ambient temperature

With hydrogenchloride; potassium permanganate; hydrazine hydrate; triethylamine; In ethanol; chloroform;

Reference yield:

: 91757-58-3
C₂₀H₁₉N₃O₃

: 52817-91-1
3,4-dihydro-5-methyl-4-oxo-1-phenyl-5H-pyridazino<4,5-b>indole

Guidance literature:: Multi-step reaction with 3 steps

1: conc. HCl / ethanol / 6 h / Heating

2: 80percent N₂H₄*H₂O / 6 h / Heating

3: 98 percent / 0.1 M KMnO₄ / CHCl₃ / 6 h / Ambient temperature

With hydrogenchloride; potassium permanganate; hydrazine hydrate; In ethanol; chloroform;