27227-40-3 Usage
Uses
Used in Organic Synthesis:
(2E)-1-(2,4-dinitrophenyl)-2-(2-methylidenebutylidene)hydrazine is used as a reactive intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2E)-1-(2,4-dinitrophenyl)-2-(2-methylidenebutylidene)hydrazine is used as a key building block in the development of new drugs. Its reactivity and structural features make it a promising candidate for the synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Development:
Similarly, in agrochemicals, (2E)-1-(2,4-dinitrophenyl)-2-(2-methylidenebutylidene)hydrazine serves as an important intermediate in the synthesis of new pesticides and other agricultural chemicals. Its potential to form a variety of chemical products makes it useful in developing more effective and targeted agrochemicals for crop protection and other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 27227-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,2 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27227-40:
(7*2)+(6*7)+(5*2)+(4*2)+(3*7)+(2*4)+(1*0)=103
103 % 10 = 3
So 27227-40-3 is a valid CAS Registry Number.
27227-40-3Relevant academic research and scientific papers
Quantitative RP-HPLC determination of some aldehydes and hydroxyaldehydes as their 2,4-dinitrophenylhydrazone derivatives
Koivusalmi,Haatainen,Root
, p. 86 - 91 (2007/10/03)
A high-performance liquid chromatographic (HPLC) method is described for the quantitative determination of some aliphatic aldehydes and β- hydroxyaldehydes as their 2,4-dinitrophenylhydrazone derivatives. A method is described for the preparation of deriv
SYNTHESIS AND REACTIONS OF SUBSTITUTED ACROLEINS.
Saprygina,Zlot-skii,Rakhmankulov
, p. 862 - 866 (2007/10/02)
In this work we examined methods for obtaining 2-alkylacroleins and their derivatives that would render these compounds as cheap and readily available products of organic synthesis. Using aldehydes we show that ethylene glycol, glycerin, and pentaerythritol in the presence of acid catalysts react primarily at the carbonyl group. Maximal yields (50-80%) were obtained when using the cation exchanger KU-2 as the acid catalyst, which also simplified the isolation of the desired products. The 2-alkyl-1,3-dioxacyclanes obtained are of particular interest as monomers, comonomers, and intermediate products of organic synthesis.
