2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione

Base Information

Chemical Name:2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione
CAS No.:110719-12-5
Molecular Formula:C16H15NS
Molecular Weight:253.368
Hs Code.:
DSSTox Substance ID:DTXSID60552737
Wikidata:Q82433105
Mol file:110719-12-5.mol

Synonyms:110719-12-5;2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione;DTXSID60552737

Suppliers and Price of 2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione

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
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Total 0 raw suppliers

Chemical Property of 2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:253.09252066
Heavy Atom Count:18
Complexity:296

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(C(=S)C2=CC=CC=C21)CC3=CC=CC=C3

Technology Process of 2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione

There total 4 articles about 2-Benzyl-3,4-dihydroisoquinoline-1(2H)-thione 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: 70.0%

: 13605-95-3
N-benzyl-1,2,3,4-tetrahydroisoquinoline

: 110719-12-5
2-Benzyl-3,4-dihydro-2H-isoquinoline-1-thione

: 342812-83-3
2-benzyl-1(2H)-thioisoquinolone

Guidance literature:: With potassium sulfide; tris(bipyridine)ruthenium(II) dichloride hexahydrate; DBN; potassium iodide; In N,N-dimethyl-formamide; at 35 ℃; for 12h; Overall yield = 19.5 mg; regioselective reaction; Inert atmosphere; Irradiation;
DOI:10.1002/cjoc.201900360

Reference yield: 63.0%

: 84500-82-3
2-benzyl-3,4-dihydroisoquinolin-2-ium bromide

: 110719-12-5
2-Benzyl-3,4-dihydro-2H-isoquinoline-1-thione

Guidance literature:: With potassium sulfide; tris(bipyridine)ruthenium(II) dichloride hexahydrate; DBN; potassium iodide; In N,N-dimethyl-formamide; at 35 ℃; for 12h; Inert atmosphere; Irradiation;
DOI:10.1002/cjoc.201900360