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Benzenesulfenamide, 2,4-dinitro-N-(2,3,5-trichloro-4-oxo-2,5-cyclohexadien-1-ylidene)-, is a complex organic compound with the chemical formula C12H5Cl3N2O5S. It is a derivative of benzenesulfenamide, featuring a 2,4-dinitro group attached to the benzene ring, and a 2,3,5-trichloro-4-oxo-2,5-cyclohexadien-1-ylidene moiety connected to the nitrogen atom. Benzenesulfenamide, 2,4-dinitro-N-(2,3,5-trichloro-4-oxo-2,5-cyclohexadien-1-ylidene)- is known for its potential applications in the synthesis of various chemical products and may have uses in the pharmaceutical or chemical industries. Due to its complex structure and specific functional groups, it is important to handle Benzenesulfenamide, 2,4-dinitro-N-(2,3,5-trichloro-4-oxo-2,5-cyclohexadien-1-ylidene)- with care, as it may exhibit hazardous properties.

89320-06-9

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89320-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89320-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89320-06:
(7*8)+(6*9)+(5*3)+(4*2)+(3*0)+(2*0)+(1*6)=139
139 % 10 = 9
So 89320-06-9 is a valid CAS Registry Number.

89320-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-2,4-Dinitrophenylthio-2,3,6-trichloro-1,4-benzoquinone imine

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

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More Details:89320-06-9 SDS

89320-06-9Downstream Products

89320-06-9Relevant academic research and scientific papers

REACTION OF N-ARYLTHIO-1,4-BENZOQUINONE IMINES WITH CHLORINE

Kolesnikov, V.T.,Vid, L.V.,Dolenko, G.N.,Kuz'menko, L.O.,Pirozhenko, V.V.,Boldeskul, I.E.

, p. 555 - 562 (2007/10/02)

In the reaction of N-arylthio-1,4-benzoquinone imines containing two potential reaction centers, i.e., the quinonoid ring and the =C=N-S- triad, with chllorine the products from chlorination of the quinonoid ring were isolated.On the basis of the experimental data a scheme is proposed for the chlorination of N-arylthio-1,4-benzoquinone imines.The electron-withdrawing characteristics of substituents in the arylthio group determine the degree of chlorination of the quinonoid ring.By x-ray fluorescence spectroscopy (XF spectroscopy) some parameters of the electronic structure of the sulfur atom and the effect of substituents in the arylthio group were determined for the N-arylthio-1,4-benzoquinone imines.

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