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Amidogen, 9H-carbazol-9-yl(2,4,6-trinitrophenyl)-, also known as 9H-carbazole-9-yl(2,4,6-trinitrophenyl)amidogen, is a complex organic compound with the chemical formula C17H9N7O6. It is characterized by the presence of a carbazole moiety, which is a tricyclic aromatic compound, and a 2,4,6-trinitrophenyl group, which is a highly energetic and reactive component. Amidogen, 9H-carbazol-9-yl(2,4,6-trinitrophenyl)- is of interest in the field of chemistry due to its potential applications in the synthesis of advanced materials and as a building block for the development of new compounds with specific properties. The structure of Amidogen, 9H-carbazol-9-yl(2,4,6-trinitrophenyl)-, features a nitrogen atom bonded to both the carbazole and trinitrophenyl groups, which contributes to its reactivity and potential use in various chemical reactions.

3685-38-9

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3685-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3685-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,8 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3685-38:
(6*3)+(5*6)+(4*8)+(3*5)+(2*3)+(1*8)=109
109 % 10 = 9
So 3685-38-9 is a valid CAS Registry Number.

3685-38-9SDS

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 9H-carbazol-9-yl(2,4,6-trinitrophenyl)-Amidogen

1.2 Other means of identification

Product number -
Other names 9-amino-N-picrylcarbazyl

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:3685-38-9 SDS

3685-38-9Relevant academic research and scientific papers

Synthesis and spectral comparison of electronic and molecular properties of some hydrazines and hydrazyl free radicals

Ionita, Petre,Lete, Cecilia,Madalan, Augustin,Matache, Mihaela,Patrascu, Bianca,Paun, Anca,Popescu, Codruta

, (2020/08/28)

Continuing our work on hydrazyl free radicals, five triphenylhydrazine derivatives, one a new compound, were synthesized to compare the electronic and molecular properties of these compounds, study the influence of substituents on the phenyl rings, and compare their properties with the parent hydrazines and corresponding anions. These hydrazines demonstrate both acid-base and redox properties. The hydrazine proton can be removed by base, yielding the corresponding anion and both the hydrazines and their anions can be oxidized to the corresponding hydrazyl free radicals. ESR spectra confirmed their formation and X-ray crystallography of one compound confirmed their structures.

Synthesis based on 9-amino-N-picrylcarbazyl

Ionita,Caproiu,Meghea,Maior,Rovinaru,Ionita

, p. 1177 - 1183 (2007/10/03)

Starting from 9-amino-N-picrylcarbazole, the nitro-, cyano-, bromo- and dibromo-derivatives of the title compound, and the corresponding free radicals, were synthesized. The pKa values and the redox properties of the compounds synthesized were reported.

Preparation of 2,2-diaryl-1-picrylhydrazyls using potassium permanganate

Brown, K. C.,Weil, J. A.

, p. 1836 - 1838 (2007/10/02)

Potessium permanganate is used as a reagent for the oxidation of various 2,2-diaryl-1-picrylhydrazines to their corresponding hydrazyls.Thin-layer chromatography indicates complete oxidation of the hydrazine to free radical, unlike the case with PbO2 (the most widely used oxidant for this purpose).Several other advantages over previous oxidants used to produce the hydrazyls are offered.

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