3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol

Base Information

Chemical Name:3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol
CAS No.:79492-42-5
Molecular Formula:C₁₆H₁₆N₂O
Molecular Weight:252.316
Hs Code.:
NSC Number:321143
DSSTox Substance ID:DTXSID20429759

Synonyms:NSC321143;79492-42-5;DTXSID20429759;NSC-321143

Suppliers and Price of 3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol

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 4 raw suppliers

Chemical Property of 3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol

Chemical Property:

Vapor Pressure:6E-10mmHg at 25°C
Boiling Point:482.9°Cat760mmHg
Flash Point:245.8°C
Density:1.16g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:252.126263138
Heavy Atom Count:19
Complexity:318

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CC2=CC=CC=C21)N=CC3=CC(=CC=C3)O
Isomeric SMILES:C1CN(CC2=CC=CC=C21)/N=C/C3=CC(=CC=C3)O

Technology Process of 3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol

There total 2 articles about 3-[(E)-3,4-dihydro-1H-isoquinolin-2-yliminomethyl]phenol 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: 42.0%

: 79492-26-5
2-amino-1,2,3,4-tetrahydro-isoquinoline-hydrochloride

: 100-83-4
meta-hydroxybenzaldehyde

: 79492-42-5
N-(m-hydroxybenzylidene)amino-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With acetic acid; Heating;

Reference yield:

: 38256-56-3
1-(2-bromo-ethyl)-2-bromomethyl-benzene

: 79492-42-5
N-(m-hydroxybenzylidene)amino-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent / triethylamine / dimethylformamide / 50 - 60 °C

2: 43 percent / conc. HCl / 40 °C

3: 42 percent / gl. acetic acid / Heating

With hydrogenchloride; acetic acid; triethylamine; In N,N-dimethyl-formamide;