4(1H)-Quinolinone, 8-amino-2,3-dihydro-

Base Information

Chemical Name:4(1H)-Quinolinone, 8-amino-2,3-dihydro-
CAS No.:50349-91-2
Molecular Formula:C9H10N2O
Molecular Weight:162.191
Hs Code.:
DSSTox Substance ID:DTXSID80485770
Wikidata:Q82325259
Mol file:50349-91-2.mol

Synonyms:50349-91-2;4(1H)-Quinolinone, 8-amino-2,3-dihydro-;8-AMINO-2,3-DIHYDROQUINOLIN-4(1H)-ONE;8-amino-2,3-dihydro-4(1H)-quinolinone;8-AMINO-2,3-DIHYDRO-1H-QUINOLIN-4-ONE;SCHEMBL6829181;DTXSID80485770;HQPFPBRBRITWKJ-UHFFFAOYSA-N;8-amino-2,3-dihydro-4(1H) -quinolinone

Suppliers and Price of 4(1H)-Quinolinone, 8-amino-2,3-dihydro-

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
Packaging
price

Labseeker
8-amino-2,3-dihydroquinolin-4(1H)-one 95
10g
$ 2200.00

American Custom Chemicals Corporation
8-AMINO-2,3-DIHYDROQUINOLIN-4(1H)-ONE 95.00%
5MG
$ 498.97

AccelPharmtech
8-amino-2,3-dihydroquinolin-4(1H)-one 97.00%
25G
$ 6000.00

AccelPharmtech
8-amino-2,3-dihydroquinolin-4(1H)-one 97.00%
5G
$ 3230.00

AccelPharmtech
8-amino-2,3-dihydroquinolin-4(1H)-one 97.00%
1G
$ 1890.00

Total 2 raw suppliers

Chemical Property of 4(1H)-Quinolinone, 8-amino-2,3-dihydro-

Chemical Property:

PSA：55.12000
LogP:1.98630
XLogP3:0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:162.079312947
Heavy Atom Count:12
Complexity:193

Purity/Quality:

99% ^*data from raw suppliers

8-amino-2,3-dihydroquinolin-4(1H)-one 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CNC2=C(C1=O)C=CC=C2N

Technology Process of 4(1H)-Quinolinone, 8-amino-2,3-dihydro-

There total 4 articles about 4(1H)-Quinolinone, 8-amino-2,3-dihydro- 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:

: 50349-89-8
8-nitro-2,3-dihydroquinoline-4(1H)-one

: 50349-91-2
1,2,3,4-tetrahydro-4-oxo-8-aminoquinoline

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; for 16h; under 760.051 Torr;

Reference yield:

: 33141-24-1
o-nitrobenzene

: 50349-91-2
1,2,3,4-tetrahydro-4-oxo-8-aminoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / water / 1.5 h / 130 °C

1.2: pH 3

2.1: phosphorus pentoxide / toluene / 2 h / Heating / reflux

3.1: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 760.05 Torr

With potassium hydroxide; hydrogen; phosphorus pentoxide; palladium 10% on activated carbon; In methanol; water; toluene;

Reference yield:

: 88-74-4
2-nitro-aniline

: 50349-91-2
1,2,3,4-tetrahydro-4-oxo-8-aminoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-benzyl-trimethylammonium hydroxide / ethanol / 29 h / 80 °C

2.1: potassium hydroxide / water / 1.5 h / 130 °C

2.2: pH 3

3.1: phosphorus pentoxide / toluene / 2 h / Heating / reflux

4.1: hydrogen / palladium 10% on activated carbon / methanol / 16 h / 760.05 Torr

With potassium hydroxide; hydrogen; phosphorus pentoxide; N-benzyl-trimethylammonium hydroxide; palladium 10% on activated carbon; In methanol; ethanol; water; toluene;