NAPHTH(2,3-h)ISOQUINOLINE

Base Information

Chemical Name:NAPHTH(2,3-h)ISOQUINOLINE
CAS No.:25082-33-1
Molecular Formula:C₁₇H₁₁N
Molecular Weight:229.281
Hs Code.:
DSSTox Substance ID:DTXSID50179775
Nikkaji Number:J1.879.642B
Wikidata:Q83050295
Mol file:25082-33-1.mol

Synonyms:NAPHTH(2,3-h)ISOQUINOLINE;CCRIS 1599;2-Azabenz(a)anthracene;25082-33-1;2-Azabenz[a]anthracene;BRN 4413709;2-Azabenzo[a]anthracene;DTXSID50179775;LS-95256

Suppliers and Price of NAPHTH(2,3-h)ISOQUINOLINE

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 0 raw suppliers

Chemical Property of NAPHTH(2,3-h)ISOQUINOLINE

Chemical Property:

Vapor Pressure:2.39E-08mmHg at 25°C
Boiling Point:464.1°C at 760 mmHg
Flash Point:213.2°C
Density:1.239g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:229.089149355
Heavy Atom Count:18
Complexity:300

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C3C(=CC2=C1)C=CC4=C3C=NC=C4

Technology Process of NAPHTH(2,3-h)ISOQUINOLINE

There total 2 articles about NAPHTH(2,3-h)ISOQUINOLINE 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:

: 80641-40-3
N-benzyl-2-aza-1,2,3,4-tetrahydrobenz anthracene-7,12-diol

: 25082-33-1
2-Azabenz anthracene

Guidance literature:: With palladium on activated charcoal; at 200 - 340 ℃; for 2.5h; Yield given;
DOI:10.1021/jo00346a047

Reference yield:

: 80641-39-0
N-benzoyl-2-aza-1,2,3,4-tetrahydrobenz anthracene-7,12-dione

: 25082-33-1
2-Azabenz anthracene

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / tetrahydrofuran / 18 h / Heating

2: 10percent Pd/C / 2.5 h / 200 - 340 °C

With palladium on activated charcoal; lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1021/jo00346a047