13483-31-3 Usage
Description
ACETONE DIMETHYLHYDRAZONE, also known as ADH, is an organic compound that serves as a versatile reagent in various chemical reactions. It is characterized by its ability to participate in hydrazone oxidation, metalation, alkylation, and condensation reactions, making it a valuable tool in the field of organic chemistry.
Uses
Used in Research and Development:
ACETONE DIMETHYLHYDRAZONE is used as a research reagent for facilitating hydrazone oxidation, metalation, alkylation, and condensation reactions. Its versatility in these reactions makes it a valuable asset in the development of new compounds and materials.
Used in Chemical Synthesis:
In the chemical synthesis industry, ACETONE DIMETHYLHYDRAZONE is used as a reagent to promote various chemical reactions, such as oxidation, metalation, alkylation, and condensation. This allows for the creation of a wide range of compounds with potential applications in various fields, including pharmaceuticals, materials science, and more.
Used in Pharmaceutical Development:
ACETONE DIMETHYLHYDRAZONE is also utilized in the pharmaceutical industry as a reagent for the synthesis of new drug candidates. Its ability to participate in various chemical reactions enables the development of novel compounds with potential therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 13483-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13483-31:
(7*1)+(6*3)+(5*4)+(4*8)+(3*3)+(2*3)+(1*1)=93
93 % 10 = 3
So 13483-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2/c1-5(2)6-7(3)4/h1-4H3
13483-31-3Relevant articles and documents
Method development for the determination of 1,1-dimethylhydrazine by the high-performance liquid chromatography–mass spectrometry technique
Susinskis, Igors,Mekss, Peteris,Hmelnickis, Juris
, p. 352 - 359 (2018/07/31)
Unsymmetrical dimethyl hydrazine is highly toxic, carcinogenic compound, widely used for organic synthesis and drug development. Therefore, due to its high reactivity, direct analysis is problematic. Current study proposes to use derivatization reaction t
Stereoselective divergent synthesis of 1,2-aminoalcohol-containing heterocycles from a common chiral nonracemic building block
Géant, Pierre-Yves,Grenet, Erwann,Martínez, Jean,Salom-Roig, Xavier J.
, p. 22 - 30 (2015/12/31)
γ-N,N-Dibenzylamino-β-hydroxysulfoxide 1 proved to be an excellent chiral building block for the synthesis of a range of 1,2-amino alcohol-containing heterocycles. Thus, 1 was converted into 4,5-disubstuted oxazolidin-2-one 4 and aminoepoxides 2 and 3. Aminoepoxide 2 proved to be an excellent precursor to access oxazolidin-2-one 5 and azetidin-3-ol 6. Finally, 2 was used as a key intermediate that allowed the development of a divergent strategy to access cis-2-methyl-6-substituted piperidin-3-ol alkaloids. (+)-Deoxocassine 7 and a C-6 ethyl analogue 8 were prepared to illustrate this approach and to demonstrate that this strategy should be adaptable to the production of other members of this alkaloid family.
Imidotitanium complexes as hydroamination catalysts: Substantially enhanced reactivity from an unexpected cyclopentadienide/amide ligand exchange
Johnson,Bergman
, p. 2923 - 2924 (2007/10/03)
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