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N-(2,6-dimethylheptan-4-ylideneamino)-2,4-dinitro-aniline is a complex organic compound with the chemical formula C17H21N5O4. It is characterized by a 2,4-dinitroaniline group attached to a 2,6-dimethylheptan-4-ylidene moiety, which contributes to its unique chemical structure. N-(2,6-dimethylheptan-4-ylideneamino)-2,4-dinitro-aniline is known for its potential applications in various chemical and industrial processes, particularly in the synthesis of dyes and pigments. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the nitro groups and the aliphatic chain, making it a compound of interest for further research and development in the field of organic chemistry.

5335-89-7

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5335-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5335-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5335-89:
(6*5)+(5*3)+(4*3)+(3*5)+(2*8)+(1*9)=97
97 % 10 = 7
So 5335-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N4O4/c1-10(2)7-12(8-11(3)4)16-17-14-6-5-13(18(20)21)9-15(14)19(22)23/h5-6,9-11,17H,7-8H2,1-4H3

5335-89-7SDS

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-(2,6-dimethylheptan-4-ylideneamino)-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-heptan-4-on-(2,4-dinitro-phenylhydrazon)

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:5335-89-7 SDS

5335-89-7Relevant academic research and scientific papers

Kinetics and mechanism of oxidation of aliphatic secondary alcohols by benzyltrimethylammonium chlorobromate

Sharma, Pradeep K.

, p. 2702 - 2706 (2014/06/09)

Oxidation of several secondary alcohols by benzyltrimethylammonium chlorobromate (BTMACB) in aqueous acetic acid leads to the formation of corresponding ketones. The reaction is first order with respect to BTMACB and the alcohols. The reaction failed to induce the polymerization of acrylonitrile. There is no effect of tetrabutylammonium chloride on the reaction rate. The proposed reactive oxidizing species is chlorobromate ion. The oxidation of benzhydrol-α-d (PhCDOHPh) exhibited a substantial primary kinetic isotope effect (kH/kD = 5.61 at 298 K). The effect of solvent composition indicated that the rate increases with an increase in the polarity of the solvent. The reaction is susceptible to both the polar and steric effects of the substituents. A mechanism involving transfer of a hydride ion in the ratedetermining step has been proposed.

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