(1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:(1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline
CAS No.:57680-86-1
Molecular Formula:C16H17N
Molecular Weight:223.318
Hs Code.:
DSSTox Substance ID:DTXSID30360922
Nikkaji Number:J956.452G
Wikidata:Q82142947

Synonyms:57680-86-1;(1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline;SCHEMBL5284097;DTXSID30360922;(S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of (1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline

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 3 raw suppliers

Chemical Property of (1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:223.136099547
Heavy Atom Count:17
Complexity:232

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CNC(C2=CC=CC=C21)CC3=CC=CC=C3
Isomeric SMILES:C1CN[C@H](C2=CC=CC=C21)CC3=CC=CC=C3

Technology Process of (1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline

There total 28 articles about (1S)-1-Benzyl-1,2,3,4-tetrahydroisoquinoline 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: 92.0%

: 132302-54-6
(1S,1'R)-1-benzyl-2-(2-hydroxy-1-phenylethyl)-1,2,3,4-tetrahydroisoquinoline

: 57680-86-1
(1S)-1-benzyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1016/S0040-4020(01)87916-3

Reference yield: 88.0%

: 350678-51-2
(S)-1-Benzyl-3,4-dihydro-1H-isoquinoline-2-carbaldehyde

: 57680-86-1
(1S)-1-benzyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With hydrogenchloride; In ethanol; for 30h; Heating;
DOI:10.1248/cpb.46.430

Reference yield: 70.0%

: [1-((S)-1-Benzyl-3,4-dihydro-1H-isoquinolin-2-yl)-meth-(E)-ylidene]-((R)-2-phenyl-2-trimethylsilanyloxy-1-trimethylsilanyloxymethyl-ethyl)-amine

: 57680-86-1
(1S)-1-benzyl-1,2,3,4-tetrahydroisoquinoline

: 57680-87-2
(1R)-1-benzyl-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With hydrazine hydrate; acetic acid; In ethanol; Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1016/S0040-4020(01)82421-2