6-Chloro-1,2,3,4-tetrahydroquinoline

Base Information

Chemical Name:6-Chloro-1,2,3,4-tetrahydroquinoline
CAS No.:49716-18-9
Molecular Formula:C9H10ClN
Molecular Weight:167.638
Hs Code.:2933499090
European Community (EC) Number:837-372-6
DSSTox Substance ID:DTXSID70457880
Nikkaji Number:J306.172H
Wikidata:Q82280921
Mol file:49716-18-9.mol

Synonyms:6-chloro-1,2,3,4-tetrahydroquinoline;49716-18-9;6-chloro-1,2,3,4-tetrahydro-quinoline;Quinoline, 6-chloro-1,2,3,4-tetrahydro-;SCHEMBL1091532;DTXSID70457880;PASUADIMFGAUDB-UHFFFAOYSA-N;MFCD09034966;AKOS000143150;MB06841;SS-4320;AM20040568;CS-0093764;FT-0682636;EN300-35412;A15597;6-chloro-1,2,3,4-tetrahydroquinoline, AldrichCPR;J-518487;Z259727454

Suppliers and Price of 6-Chloro-1,2,3,4-tetrahydroquinoline

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

TRC
6-Chloro-1,2,3,4-tetrahydroquinoline
250mg
$ 125.00

SynQuest Laboratories
6-Chloro-1,2,3,4-tetrahydroquinoline 98%
250 mg
$ 176.00

SynQuest Laboratories
6-Chloro-1,2,3,4-tetrahydroquinoline 98%
1 g
$ 280.00

SynQuest Laboratories
6-Chloro-1,2,3,4-tetrahydroquinoline 98%
5 g
$ 832.00

Medical Isotopes, Inc.
6-Chloro-1,2,3,4-tetrahydroquinoline 95+%
1 g
$ 500.00

Matrix Scientific
6-Chloro-1,2,3,4-tetrahydroquinoline >95%
500mg
$ 91.00

Matrix Scientific
6-Chloro-1,2,3,4-tetrahydroquinoline >95%
1g
$ 139.00

Labseeker
6-chloro-1,2,3,4-tetrahydroquinoline 95
5g
$ 616.00

Crysdot
6-Chloro-1,2,3,4-tetrahydroquinoline 95+%
5g
$ 404.00

Chemenu
6-Chloro-1,2,3,4-tetrahydroquinoline 95%
1g
$ 143.00

Total 33 raw suppliers

Chemical Property of 6-Chloro-1,2,3,4-tetrahydroquinoline

Chemical Property:

Vapor Pressure:0.00239mmHg at 25°C
Boiling Point:288.1oC at 760 mmHg
Flash Point:128oC
PSA：12.03000
Density:1.162g/cm3
LogP:2.83610
Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:167.0501770
Heavy Atom Count:11
Complexity:138

Purity/Quality:

99%, ^*data from raw suppliers

6-Chloro-1,2,3,4-tetrahydroquinoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=C(C=CC(=C2)Cl)NC1
Uses 6-Chloro-1,2,3,4-tetrahydroquinoline (cas# 49716-18-9) is a compound useful in organic synthesis.

Technology Process of 6-Chloro-1,2,3,4-tetrahydroquinoline

There total 6 articles about 6-Chloro-1,2,3,4-tetrahydroquinoline 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:

: 612-57-7
6-chloroquinoline

: 49716-18-9
6-chloro-1,2,3,4-tetrahydroquinoline

: 767-92-0,10343-99-4,22160-37-8,22160-38-9,105728-23-2,115730-30-8,115730-31-9,150254-00-5,2051-28-7
decahydroquinoline

Guidance literature:: With hydrogen; In neat (no solvent); at 100 ℃; for 2h; under 3750.38 Torr; Autoclave; Sealed tube;
DOI:10.1016/j.catcom.2019.02.019

Reference yield:

: 612-57-7
6-chloroquinoline

: 635-46-1
1,2,3,4-tetrahydroisoquinoline

: 49716-18-9
6-chloro-1,2,3,4-tetrahydroquinoline

: 767-92-0,10343-99-4,22160-37-8,22160-38-9,105728-23-2,115730-30-8,115730-31-9,150254-00-5,2051-28-7
decahydroquinoline

Guidance literature:: With platinum on activated charcoal; hydrogen; In methanol; at 110 ℃; for 3h; under 22502.3 Torr; Reagent/catalyst; Autoclave;
DOI:10.1021/acscatal.6b01240

Reference yield:

: 612-57-7
6-chloroquinoline

: 91-22-5
quinoline

: 635-46-1
1,2,3,4-tetrahydroisoquinoline

: 49716-18-9
6-chloro-1,2,3,4-tetrahydroquinoline

: C₉H₁₆ClN

Guidance literature:: With palladium on activated charcoal; hydrogen; In isopropyl alcohol; at 80 ℃; for 2h; Reagent/catalyst; Autoclave;
DOI:10.1016/j.chempr.2020.07.023