4864-46-4 Usage
Description
1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine is a hydrazine derivative with the molecular formula C14H16N4O4, featuring a dinitrophenyl group and a 3-methylcyclohexylidene group. This chemical compound is recognized for its explosive properties and is utilized in organic synthesis and as a reagent in various chemical reactions. It also serves as a precursor in the synthesis of other compounds and holds potential in the pharmaceutical industry for developing new drugs and pharmaceuticals. However, its explosive nature and potential health hazards necessitate careful handling.
Uses
Used in Organic Synthesis:
1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine is used as a reagent in organic synthesis for [application reason], contributing to the formation of complex organic molecules and facilitating specific chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine is used as a building block for the synthesis of new drugs and pharmaceutical compounds due to its unique chemical structure and reactivity.
Used in Chemical Reactions:
1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine is employed as a reagent in chemical reactions, where its explosive properties and specific functional groups enable it to participate in various reaction mechanisms, leading to the formation of desired products.
Used as a Precursor in Synthesis:
1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine is also used as a precursor in the synthesis of other compounds, highlighting its versatility and importance in the field of chemistry.
Caution:
Due to its explosive nature and potential health hazards, 1-(2,4-dinitrophenyl)-2-(3-methylcyclohexylidene)hydrazine requires careful handling and proper safety measures during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4864-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4864-46:
(6*4)+(5*8)+(4*6)+(3*4)+(2*4)+(1*6)=114
114 % 10 = 4
So 4864-46-4 is a valid CAS Registry Number.
4864-46-4Relevant articles and documents
A modification of a conventional technique for the synthesis of hydrazones of racemic carbonyls: Prevention of spontaneous chiral inversion
Singh, Manisha,Bhushan, Ravi
, p. 105719 - 105726 (2015/12/30)
Conventionally hydrazones and other derivatives of carbonyls are synthesized under acidic conditions when spontaneous chiral inversion is a common problem if the carbonyl compound is chiral. A new method has been developed involving solid phase microwave-assisted conditions for the synthesis of 2,4-dinitrophenyl hydrazone(s) of chiral carbonyl compounds wherein there occurred no inversion of configuration. The method provided high yields (91-95%) in short reaction times (4-6 min). The method proposed clearly has synthetic advantages over current practices. The hydrazones were characterized by IR, 1H NMR and CHN analysis. The hydrazones represent enantiomeric pairs tagged with a strong chromophore rather than diastereomers. The enantiomeric pairs were separated by HPLC using an α1-acid glycoprotein column and the best resolution of all the analytes was achieved with a mobile phase containing 0.5% 2-propanol in 10 mM citrate phosphate buffer at pH 6.5. The chromatographic peaks clearly showed base line separation with comparable peak areas and thus the results confirmed that there was no spontaneous inversion of configuration during derivatization. The chromatograms corresponding to the products obtained by conventional procedure (from the racemic mixtures of analytes) showed peaks with unequal areas suggesting formation of enantiomers in unequal amounts (i.e., non racemic mixtures) because of spontaneous inversion of the configuration during derivatization.
