92304-54-6 Usage
Uses
Used in Pharmaceutical Industry:
Hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) is used as a reagent in organic synthesis for the production of pharmaceuticals. Its versatility in chemical reactions allows for the development of new drugs and materials, contributing to the advancement of medicinal chemistry.
Used in Pesticide Industry:
In the pesticide industry, Hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) is utilized as a reagent in the synthesis of various pesticides. Its ability to participate in different chemical reactions enables the creation of effective and innovative pest control agents.
Used in Research and Development:
Hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) serves as a valuable building block in the preparation of various heterocyclic compounds, which are essential in the field of organic chemistry. Its application in research and development facilitates the discovery and synthesis of novel compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 92304-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92304-54:
(7*9)+(6*2)+(5*3)+(4*0)+(3*4)+(2*5)+(1*4)=116
116 % 10 = 6
So 92304-54-6 is a valid CAS Registry Number.
92304-54-6Relevant academic research and scientific papers
Schmidt, Michael A.
, p. 1941 - 1960 (2022)
The effect of alkylation on the terminal position of aryl and heteroaryl hydrazines in the Fischer indole synthesis was examined. Compared to their unalkylated counterparts, reactions using alkylated hydrazines provided indole products with higher yields and faster rates. The reactions can be conducted at lower temperatures and are compatible with acid-sensitive functionality. The terminally alkylated hydrazines were readily prepared by a new two-step sequence and held as stable hydrazinium salts. The mild formation of the salts along with the favorable Fischer indole reaction conditions highlights the potential of this approach in later-stage synthetic use.
