19796-84-0 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Pentanediimine is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to form stable complexes with other molecules makes it a valuable component in the development of new drugs and medicinal compounds.
Used in Chemical Industry:
In the chemical industry, 2,4-Pentanediimine serves as a crosslinking agent in the production of polymers and resins. Its reactivity allows for the formation of strong bonds between polymer chains, enhancing the overall strength and stability of the resulting materials.
Used as a Reagent in Organic Synthesis:
2,4-Pentanediimine is utilized as a reagent in organic synthesis for the preparation of a wide range of nitrogen-containing compounds. Its unique chemical properties enable the creation of complex organic molecules that are used in various applications, including the development of new chemical products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 19796-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19796-84:
(7*1)+(6*9)+(5*7)+(4*9)+(3*6)+(2*8)+(1*4)=170
170 % 10 = 0
So 19796-84-0 is a valid CAS Registry Number.
19796-84-0Relevant academic research and scientific papers
Synergism by sublimation of volatile lanthanide β-diketonates
Kuzmina, Natalia P.,Martynenko, Larissa I.,Chugarov, Nikolai V.,Zaitseva, Irina G.,Grigoriev, Andrei N.,Yakushevich, Andrei N.
, p. 158 - 162 (2008/10/08)
The synergistic effect by sublimation manifests itself in an increase in the volatility of nonvolatile or slightly volatile compounds in the presence of highly volatile agents. In this study, manifestations of the synergistic effect are demonstrated by th
RADICAL-ION PERFLUOROALKYLATION. VIII. REACTION OF PERFLUOROALKYL IODIDES WITH β-DIKETONES IN LIQUID AMMONIA
Yagupol'skii, L. M.,Matyushecheva, G. I.,Pavlenko, N. V.,Boiko, V. N.
, p. 10 - 14 (2007/10/02)
During the UV irradiation of perfluoroalkyl iodides with acetyl-, pivaloyl-, and benzoyl-acetone in liquid ammonia C-perfluoroalkylation of the β-diketones occurs with subsequent ammonolysis of the CF2 group at the α position to the carbanionic center.The acetyl group is removed, and β-perfluoroalkyl-β-aminovinyl ketones are formed.Trifluoroacetylacetone reacts similarly, but the CF3CO group is removed.The cyano derivative of the β-aminovinyl ketone, on which the acetyl group is preserved, was isolated from the products from the reaction of acetylacetone with trifluoroiodomethane.
