7153-35-7 Usage
Description
1-(2,4-dimethylpentan-3-ylidene)-2-(2,4-dinitrophenyl)hydrazine is a hydrazine derivative with the molecular formula C17H25N5O4. It features a hydrazine group and a dinitrophenyl group, along with a substituted pentan-3-ylidene chain. This chemical compound is known for its ability to form stable complexes with certain metal ions, making it a valuable compound in organic synthesis and chemical research.
Uses
Used in Chemical Research and Organic Synthesis:
1-(2,4-dimethylpentan-3-ylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a reagent for detecting and identifying various organic compounds, particularly aldehydes and ketones. Its unique structure allows it to form stable complexes with metal ions, which is beneficial for a wide range of chemical analyses and reactions.
Used in Pharmaceutical Development:
1-(2,4-dimethylpentan-3-ylidene)-2-(2,4-dinitrophenyl)hydrazine is also studied for its potential as a precursor in the development of various pharmaceutical products. Its ability to interact with metal ions and its reactivity with organic compounds make it a promising candidate for the creation of new drugs.
Used in Agricultural Product Development:
In addition to pharmaceutical applications, 1-(2,4-dimethylpentan-3-ylidene)-2-(2,4-dinitrophenyl)hydrazine has been investigated for its potential use in the development of agricultural products. Its chemical properties and reactivity may contribute to the creation of new compounds that can be used in the agricultural industry.
Check Digit Verification of cas no
The CAS Registry Mumber 7153-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7153-35:
(6*7)+(5*1)+(4*5)+(3*3)+(2*3)+(1*5)=87
87 % 10 = 7
So 7153-35-7 is a valid CAS Registry Number.
7153-35-7Relevant articles and documents
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.
