5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-one

Base Information

Chemical Name:5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-one
CAS No.:51916-89-3
Molecular Formula:C17H15N3O
Molecular Weight:277.326
Hs Code.:
DSSTox Substance ID:DTXSID30492479
Mol file:51916-89-3.mol

Synonyms:51916-89-3;DTXSID30492479;5-methyl-1-phenyl-2,3-dihydro-1H-pyridazino[4,5-b]indol-4(5H)-one;5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-one

Suppliers and Price of 5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-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-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-one

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:277.121512110
Heavy Atom Count:21
Complexity:407

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CC=CC=C2C3=C1C(=O)NNC3C4=CC=CC=C4

Technology Process of 5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-one

There total 5 articles about 5-Methyl-1-phenyl-1,2,3,5-tetrahydro-4H-pyridazino[4,5-b]indol-4-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:

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

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

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / CHCl₃ / Heating

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

3: 80percent N₂H₄*H₂O / 6 h / Heating

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

Reference yield:

: 91757-58-3
C₂₀H₁₉N₃O₃

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

Guidance literature:: Multi-step reaction with 2 steps

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

2: 80percent N₂H₄*H₂O / 6 h / Heating

With hydrogenchloride; hydrazine hydrate; In ethanol;