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12-Nitroindeno(1,2,3-cd)pyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95050-14-9

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95050-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95050-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95050-14:
(7*9)+(6*5)+(5*0)+(4*5)+(3*0)+(2*1)+(1*4)=119
119 % 10 = 9
So 95050-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H11NO2/c24-23(25)18-6-2-5-15-17-11-14-4-1-3-12-7-8-13-9-10-16(21(15)18)22(17)20(13)19(12)14/h1-11H

95050-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name CCRIS 3793

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:95050-14-9 SDS

95050-14-9Upstream product

95050-14-9Downstream Products

95050-14-9Relevant academic research and scientific papers

Synthesis and Conformational Analysis of Nitropolycyclic Fluoranthenes

Cho, Bongsup P.,Kim, Misoo,Harvey, Ronald G.

, p. 5788 - 5796 (1993)

Nitroarenes are ubiquitous environmental pollutants some of which exhibit mutagenic and tumorigenic activities.The first systematic investigation of the nitration reactions of the polycyclic fluoranthenes, a major class of nonalternant polyarenes, is described.The specific hydrocarbons studied were benzacephenanthrylene (1), benzaceanthrylene (2), indenopyrene (3), indenochrysene (4), dibenzaceanthrylene (5), dibenzacenathrylene (6), and dibenzacephenanthrylene (7).The nitration of all hydrocarbons, except 1, proceeded with remarkable regioselectivity to provide a single mononitro product.In the case of 1, 17percent of a second mononitro isomer was isolated.The structures of the resulting mononitrofluoranthenes (8-15) were fully characterized by analysis of their high-resolution COSY, long-range COSY, and NOESY NMR spectra and by comparison with the spectra of the parent hydrocarbons.The observed nitration sites of the polycyclic fluoranthenes were in excellent agreement with theoretical predictions made by the DEWAR-PI method based on the relative energies of the Wheland intermediates for substitutions at various ring positions.The availability of the complete (1)H chemical shift assignments of the nitropolycyclic fluoranthenes (8-15), together with those of the parent hydrocarbons (1-7) and their UV-visible spectral data, enabled the molecular conformations of the nitro groups to be probed.

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