2(1H)-Quinolinethione, 3,4-dihydro-

Base Information

Chemical Name:2(1H)-Quinolinethione, 3,4-dihydro-
CAS No.:41493-89-4
Molecular Formula:C9H9NS
Molecular Weight:163.243
Hs Code.:
DSSTox Substance ID:DTXSID30194385
Nikkaji Number:J681.976A
Mol file:41493-89-4.mol

Synonyms:41493-89-4;2(1H)-Quinolinethione, 3,4-dihydro-;3,4-Dihydro-2(1H)-quinolinethione;SCHEMBL88725;SCHEMBL14153565;DTXSID30194385;3,4-Dihydroquinoline-2(1H)-thione

Suppliers and Price of 2(1H)-Quinolinethione, 3,4-dihydro-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2(1H)-Quinolinethione, 3,4-dihydro-

Chemical Property:

Vapor Pressure:0.00859mmHg at 25°C
Boiling Point:266.5°C at 760 mmHg
Flash Point:115°C
Density:1.22g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:163.04557046
Heavy Atom Count:11
Complexity:167

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=S)NC2=CC=CC=C21

Technology Process of 2(1H)-Quinolinethione, 3,4-dihydro-

There total 3 articles about 2(1H)-Quinolinethione, 3,4-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: 93.0%

: 553-03-7
3,4-dihydro-2(1H)-quinolone

: 41493-89-4
3,4-dihydro-(1H)-quinoline-2-thione

Guidance literature:: With Lawessons reagent; In toluene; for 0.25h; Heating;
DOI:10.1021/jo000603t

Reference yield:

: 90006-13-6
2-aminophenethyl bromide

: 41493-89-4
3,4-dihydro-(1H)-quinoline-2-thione

Guidance literature:: Multi-step reaction with 2 steps

1: palladium diacetate; sodium carbonate / toluene / 4 h / 50 °C / 1500.15 Torr / Autoclave; Inert atmosphere

2: Lawessons reagent / toluene / 10 h / Reflux

With Lawessons reagent; palladium diacetate; sodium carbonate; In toluene;