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Cyclopentanone, 2-cyclopentylidene-, 2-(2,4-dinitrophenyl)hydrazone is a complex organic compound with the chemical formula C13H14N4O4. It is a derivative of cyclopentanone, featuring a cyclopentylidene group and a 2,4-dinitrophenylhydrazone moiety. Cyclopentanone,2-cyclopentylidene-, 2-(2,4-dinitrophenyl)hydrazone is characterized by its unique structure, which includes a five-membered ring (cyclopentane) with a ketone group, a double bond, and a hydrazone functional group attached to a 2,4-dinitrophenyl group. The compound is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical compounds due to its reactive functional groups. However, it is important to note that the compound's properties, reactivity, and potential uses would require further investigation and characterization.

853-96-3

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853-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853-96-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 853-96:
(5*8)+(4*5)+(3*3)+(2*9)+(1*6)=93
93 % 10 = 3
So 853-96-3 is a valid CAS Registry Number.

853-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2-cyclopentylidenecyclopentylidene)amino]-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names 2-Oxy-dicyclopentyl

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:853-96-3 SDS

853-96-3Downstream Products

853-96-3Relevant academic research and scientific papers

Formation of 3-Substituted 2-Iminocyclopentanedithiocarboxylic Acids and N-[Amino(dimercapto)methyl]-2-methylcyclopentanimine from 2-Substituted Cyclopentanones. Some Reactions of the Imino-dithiocarboxylic Acids

Takeshima, Tatsuo,Miyauchi, Tetsuko,Fukada, Naoaki,Koshizawa, Shuichi,Muraoka, Motomu

, p. 1009 - 1013 (2007/10/09)

2-Ethyl, 2-isopropyl, 2-cyclopentyl, and 2-cyclopentylidenecyclopentanones, when treated with carbon disulphide and ammonia, gave the corresponding 3-substituted 2-iminocyclopentanedithiocarboxylic acids (5)-(7) and (9). Under the same conditions, 2-methylcyclopentanone gave 2-imino-3- methylcyclopentanedithiocarboxylic acid (2), and N-[amino(dimercapto)methyl]-2- methylcyclopentanimine (3), and 2-isopropylidenecyclopentanone gave 7a-amino-4,4-dimethylperhydrocyclopenta[e][1,3]thiazine-2-thione (8). Reactions of the 2-iminocyclopentanedithiocarboxylic acids with hydrazine, thiosemicarbazide, picryl chloride, and phenyl isothiocyanate have also been investigated.

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