54347-29-4 Usage
Uses
Used in Pharmaceutical Research:
C-(1-cyclohexyl-1H-tetrazol-5-yl)-methylamine; hydrochloride is used as a research compound for its potential role in the development of central nervous system stimulants. Its unique structure allows for exploration into how it may interact with and influence neurological processes.
Used in Drug Synthesis:
In the pharmaceutical industry, C-(1-cyclohexyl-1H-tetrazol-5-yl)-methylamine; hydrochloride serves as a pharmaceutical intermediate, playing a crucial role in the synthesis of other compounds with therapeutic potential. Its ability to be modified and incorporated into various molecular structures makes it a valuable asset in drug development.
Used in Medicinal Chemistry:
C-(1-cyclohexyl-1H-tetrazol-5-yl)-methylamine; hydrochloride is utilized as a versatile compound in medicinal chemistry, where it may contribute to the creation of new medications for a range of conditions, including chronic pain and neurological disorders. Its potential applications in this field are vast, given the compound's adaptability and the ongoing need for novel therapeutic agents.
Used in the Development of New Medications:
C-(1-cyclohexyl-1H-tetrazol-5-yl)-methylamine; hydrochloride C-(1-cyclohexyl-1H-tetrazol-5-yl)-methylamine; hydrochloride is also used in the development of new medications, particularly for conditions such as chronic pain or neurological disorders. Its unique properties and potential interactions with biological targets make it a promising candidate for further research and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 54347-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,4 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54347-29:
(7*5)+(6*4)+(5*3)+(4*4)+(3*7)+(2*2)+(1*9)=124
124 % 10 = 4
So 54347-29-4 is a valid CAS Registry Number.
54347-29-4Relevant academic research and scientific papers
5-(Diazomethyl)tetrazoles Substituted in Position 1 or 2 - A Comparative Study
Moderhack, Dietrich,Goos, Karl-Heinz
, p. 921 - 930 (2007/10/02)
The hitherto unknown title compounds 1 and 2 - readily obtained by amine diazotation (1) and Bamford-Stevens reaction (1, 2), respectively - show expected differences in both spectroscopic (UV/VIS,IR) and reactive behaviour towards (a) acids and electroph
