92304-54-6 Usage
General Description
Hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) is a chemical compound commonly used in the pharmaceutical and research industries. It is a hydrazine derivative, with the chemical formula C9H13N2?HCl. Hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) is typically used as a reagent in organic synthesis, particularly in the production of pharmaceuticals and pesticides. It is also a versatile building block for the preparation of various heterocyclic compounds. Additionally, hydrazine, 1-Methyl-2-phenyl-, hydrochloride (1:1) is known for its ability to undergo various chemical reactions, making it an important component in the development of new drugs and materials. However, it is important to handle this chemical with care as it is highly toxic and can pose serious health risks if mishandled.
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 articles and documents
Effect of Terminal Alkylation of Aryl and Heteroaryl Hydrazines in the Fischer Indole Synthesis
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.
