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1,3,6,8-tetranitro-4,9-dihydropyrido[2,3,4,5-lmn]phenanthridine-5,10-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56181-16-9

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56181-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56181-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,8 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56181-16:
(7*5)+(6*6)+(5*1)+(4*8)+(3*1)+(2*1)+(1*6)=119
119 % 10 = 9
So 56181-16-9 is a valid CAS Registry Number.

56181-16-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name NQJOEKIWOPDIOA-UHFFFAOYSA

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56181-16-9 SDS

56181-16-9Downstream Products

56181-16-9Relevant academic research and scientific papers

INVESTIGATION OF PHENANTHRIDONE AND DIOXOTETRAHYDRODIAZAPYRENE. 3. INVESTIGATION OF THE NITRATION OF 5H-PHENANTHRIDIN-6-ONE AND ITS DERIVATIVES

Migachev, G. I.,Grekhova, N. G.,Terent'ev, A. M.

, p. 289 - 294 (2007/10/02)

The nitration of 5H-phenanthridin-6-one (I), 5H-phenanthridin-6-one-10-carboxylic (II) and 5H-phenanthridin-6-one-1-carboxylic acids (III), 4H-cyclopentaphenanthridine-5,9-dione (IV), 4H-cyclopentaphenanthridine-5-one (V), 5,10-dioxo-4,5,9,10-tetrahydro-4,9-diazapyrene (VI), and 5,9-dioxo-4,5,9,10-tetrahydro-4,10-diazapyrene (VII) with nitric acid (sp. gr. 1.42-1.51) and a nitrating mixture of 0-120 deg C was investigated.The orientation and sequence of incorporation of nitro groups in I-VII are determined by the presence of a phenanthridone structure in them.Mono-, di-, tri-, and tetranitro-substituted I-VII were obtained and characterized.

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