Quinoline, 1,2,3,4-tetrahydro-1-propyl-

Base Information

Chemical Name:Quinoline, 1,2,3,4-tetrahydro-1-propyl-
CAS No.:6613-29-2
Molecular Formula:C12H17N
Molecular Weight:175.274
Hs Code.:
DSSTox Substance ID:DTXSID70425069
Wikidata:Q82237821
ChEMBL ID:CHEMBL1622331

Synonyms:6613-29-2;ChemDiv2_000871;Quinoline, 1,2,3,4-tetrahydro-1-propyl-;HMS1371H13;SCHEMBL6197333;CHEMBL1622331;DTXSID70425069;1-propyl-1,2,3,4-tetrahydroquinoline

Suppliers and Price of Quinoline, 1,2,3,4-tetrahydro-1-propyl-

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 Quinoline, 1,2,3,4-tetrahydro-1-propyl-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:175.136099547
Heavy Atom Count:13
Complexity:155

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCN1CCCC2=CC=CC=C21

Technology Process of Quinoline, 1,2,3,4-tetrahydro-1-propyl-

There total 2 articles about Quinoline, 1,2,3,4-tetrahydro-1-propyl- 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: 80.0%

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

: 504-63-2
trimethyleneglycol

: 479-59-4
julolidine

: 6613-29-2
1-propyl-1,2,3,4-tetrahydroquinoline

Guidance literature:: With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; ortho-diphenylphosphinobenzoic acid; In toluene; at 130 ℃; for 36h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Green chemistry;
DOI:10.1002/cctc.201500051

Reference yield:

: 6,7-benzo-5-aza-1-boraspiro<4,5>decane

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

: 6613-29-2
1-propyl-1,2,3,4-tetrahydroquinoline

: 88014-20-4
3-(1,2,3,4-tetrahydro-1-quinolyl)-1-propanol

Guidance literature:: With hydrogenchloride; sodium hydroxide; dihydrogen peroxide; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1) acetone, 15 min., reflux; 2) water, THF, 4 h, reflux;