Sontoquine

Base Information

Chemical Name:Sontoquine
CAS No.:85-10-9
Molecular Formula:C₁₉H₂₈ClN₃
Molecular Weight:333.904
Hs Code.:
UNII:U34E688BAM
DSSTox Substance ID:DTXSID801005318
Nikkaji Number:J10.614C
Wikidata:Q27290622
ChEMBL ID:CHEMBL343728

Synonyms:1,4-Pentanediamine, N4-(7-chloro-3-methyl-4-quinolinyl)-N1,N1-diethyl;3-methylchloroquine;7-Chloro-4-((4-(diethylamino)-1-methylbutyl)amino)-3-methylquinoline

Suppliers and Price of Sontoquine

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

Total 2 raw suppliers

Chemical Property of Sontoquine

Chemical Property:

Vapor Pressure:3.81E-09mmHg at 25°C
Boiling Point:473.8°Cat760mmHg
Flash Point:240.3°C
Density:1.097g/cm³
XLogP3:5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:333.1971756
Heavy Atom Count:23
Complexity:335

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CCCC(C)NC1=C2C=CC(=CC2=NC=C1C)Cl

Technology Process of Sontoquine

There total 7 articles about Sontoquine 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:

: 6622-28-2
4,7-dichloro-3-methylquinoline

: 140-80-7
5-diethylamino-2-pentylamine

: 85-10-9
N⁴-(7-chloro-3-methyl-4-quinolinyl)-N¹,N1-diethyl-1,4-pentanediamine

Guidance literature:: With sodium iodide; phenol;
DOI:10.1021/ja01207a011

Reference yield:

: 724734-08-1
7-chloro-4-hydroxy-3-methyl-quinoline-2-carboxylic acid

: 85-10-9
N⁴-(7-chloro-3-methyl-4-quinolinyl)-N¹,N1-diethyl-1,4-pentanediamine

Guidance literature:: Multi-step reaction with 3 steps

1: diphenyl ether / Heating

2: POCl₃ / 1 h / 100 °C

3: 1.) 100 deg C, 2 h, 2.) 145-160 deg C, 8 h

With trichlorophosphate; In diphenylether;
DOI:10.1002/jhet.5570340149

Reference yield:

: 180605-61-2
7-chloro-4-hydroxy-3-methyl-quinoline-2-carboxylic acid ethyl ester

: 85-10-9
N⁴-(7-chloro-3-methyl-4-quinolinyl)-N¹,N1-diethyl-1,4-pentanediamine

Guidance literature:: Multi-step reaction with 4 steps

1: 2 N NaOH / 1.5 h / Heating

2: diphenyl ether / Heating

3: POCl₃ / 1 h / 100 °C

4: 1.) 100 deg C, 2 h, 2.) 145-160 deg C, 8 h

With sodium hydroxide; trichlorophosphate; In diphenylether;
DOI:10.1002/jhet.5570340149