1,8-Dinitronaphthalene

Base Information Edit

Chemical Name:1,8-Dinitronaphthalene
CAS No.:602-38-0
Molecular Formula:C10H6 N2 O4
Molecular Weight:218.169
Hs Code.:2904.20
European Community (EC) Number:210-016-1
NSC Number:6323
UNII:H6D9Q0K9E6
DSSTox Substance ID:DTXSID9025166
Nikkaji Number:J3.306E
Wikidata:Q27122164
ChEMBL ID:CHEMBL167529
Mol file:602-38-0.mol

Synonyms:1,8-Dinitronaphthalene;NSC 6323

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Chemical Property of 1,8-Dinitronaphthalene Edit

Chemical Property:

Appearance/Colour:Yellow Crystalline Powder
Vapor Pressure:6.22E-06mmHg at 25°C
Melting Point:171 - 172 C (97 %)
Refractive Index:1.7040 (estimate)
Boiling Point:389.8°C at 760 mmHg
Flash Point:200.3°C
PSA：91.64000
Density:1.481g/cm³
LogP:3.70260
Water Solubility.:34mg/L(15 oC)
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:218.03275668
Heavy Atom Count:16
Complexity:268

Purity/Quality:

Safty Information:

Pictogram(s): UN NO.
Hazard Codes:F,Xi
Statements: 11-36/37/38
Safety Statements: 16-26-36

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Nitrogen Compounds -> Nitros, Aromatic
Canonical SMILES:C1=CC2=C(C(=C1)[N+](=O)[O-])C(=CC=C2)[N+](=O)[O-]
Uses 1,8-Dinitronaphthalene (cas# 602-38-0) is a compound useful in organic synthesis.

Technology Process of 1,8-Dinitronaphthalene

There total 29 articles about 1,8-Dinitronaphthalene 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: 81.0%

: 518-05-8
Naphthalene-1,8-dicarboxylic acid

: 602-38-0
1,8-dinitronaphthalene

Guidance literature:: With nitronium tetrafluoborate; silver carbonate; In N,N-dimethyl acetamide; at 90 ℃; for 12h; regioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.joc.5b02133