1-(3-Nitrophenyl)-2-quinolin-2-ylethanol

Base Information

Chemical Name:1-(3-Nitrophenyl)-2-quinolin-2-ylethanol
CAS No.:5437-26-3
Molecular Formula:C17H14 N2 O3
Molecular Weight:294.31
Hs Code.:
NSC Number:15993
DSSTox Substance ID:DTXSID60280225

Synonyms:1-(3-nitrophenyl)-2-quinolin-2-ylethanol;5437-26-3;NSC15993;DTXSID60280225;NSC 15993;NSC-15993

Suppliers and Price of 1-(3-Nitrophenyl)-2-quinolin-2-ylethanol

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 5 raw suppliers

Chemical Property of 1-(3-Nitrophenyl)-2-quinolin-2-ylethanol

Chemical Property:

Vapor Pressure:3.22E-09mmHg at 25°C
Boiling Point:459°Cat760mmHg
Flash Point:231.4°C
Density:1.335g/cm³
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:294.10044231
Heavy Atom Count:22
Complexity:385

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC(=N2)CC(C3=CC(=CC=C3)[N+](=O)[O-])O

Technology Process of 1-(3-Nitrophenyl)-2-quinolin-2-ylethanol

There total 3 articles about 1-(3-Nitrophenyl)-2-quinolin-2-ylethanol 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: 90.0%

: 91-63-4
2-methylquinoline

: 99-61-6
3-nitro-benzaldehyde

: 5437-26-3
1‐(3‐nitrophenyl)‐2‐(quinolin‐2‐yl)ethanol

Guidance literature:: With H₂O₄P^(1-)*C₄H₇N₂⁽¹⁺⁾; In 1,4-dioxane; water; at 100 ℃; for 24h; Schlenk technique; Sealed tube;
DOI:10.1016/j.tetlet.2014.08.034