55330-60-4 Usage
Uses
Used in Organic Synthesis:
1-Methylhydrazine Dihydrochloride is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic compounds.
Used in Pharmaceutical Preparation:
1-Methylhydrazine Dihydrochloride is used as a reagent in the preparation of pharmaceuticals, where its alkylating properties are utilized to modify biologically active molecules, potentially enhancing their therapeutic effects.
Used in Research Laboratories:
In research settings, 1-Methylhydrazine Dihydrochloride is used as a tool to study the effects of alkylating agents on DNA, proteins, and other biomolecules, providing insights into the mechanisms of carcinogenesis and the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 55330-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,3 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55330-60:
(7*5)+(6*5)+(5*3)+(4*3)+(3*0)+(2*6)+(1*0)=104
104 % 10 = 4
So 55330-60-4 is a valid CAS Registry Number.
InChI:InChI=1/CH6N2.2ClH/c1-3-2;;/h3H,2H2,1H3;2*1H
55330-60-4Relevant academic research and scientific papers
Process for the preparation of tertiary butyl hydrazine hydrohalogenide
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, (2008/06/13)
An industrially and economically advantageous process for the preparation of a TBH-HX using starting materials which are cheaply available and are easy to handle, maintaining a high yield. A tertiary butyl hydrazine hydrohalogenide is prepared by reacting a hydrazine hydrohalogenide with a methyl tertiary butyl ether in the presence of an acid.
1,1,4,4,-TETRAALKYLAMIDAZINES. SYNTHESIS OF MONOALKYLHYDRAZINES
Zelenin, K. N.,Khrustalev, V. A.,Sergutina, V. P.
, p. 244 - 247 (2007/10/02)
A series of 1,1,4,4,-tetraalkylamidazines were synthesized.Their IR, UV, and 1H and 13C NMR spectra were investigated, and the characteristics of their stereochemical structure are discussed.Amidazines are alkylated by the action of alkyl iodides at the imine nitrogen atom.Alkaline cleavage of the alkyl iodide derivatives is a method for the production of monoalkylhydrazines.
