60764-18-3 Usage
Uses
Used in Laboratory Research:
Pyridinium, 3-[(hydroxyimino)methyl]-1-(phenylmethyl)-, bromide is used as a reagent in organic synthesis reactions for its catalytic and intermediate properties, facilitating the preparation of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Pyridinium, 3-[(hydroxyimino)methyl]-1-(phenylmethyl)-, bromide is utilized as a catalyst or intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Pyridinium, 3-[(hydroxyimino)methyl]-1-(phenylmethyl)-, bromide is employed as a reagent in the synthesis of agrochemicals, aiding in the production of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Material Science:
In material science, Pyridinium, 3-[(hydroxyimino)methyl]-1-(phenylmethyl)-, bromide is used as a component in the development of new materials with specific properties, such as conductivity, stability, or reactivity, for various applications in industries like electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 60764-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,6 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60764-18:
(7*6)+(6*0)+(5*7)+(4*6)+(3*4)+(2*1)+(1*8)=123
123 % 10 = 3
So 60764-18-3 is a valid CAS Registry Number.
60764-18-3Relevant academic research and scientific papers
New safe method for preparation of sarin-exposed human erythrocytes acetylcholinesterase using non-toxic and stable sarin analogue isopropyl p-nitrophenyl methylphosphonate and its application to evaluation of nerve agent antidotes
Ohta, Hikoto,Ohmori, Takeshi,Suzuki, Shinichi,Ikegaya, Hiroshi,Sakurada, Koichi,Takatori, Takehiko
, p. 2827 - 2833 (2007/10/03)
Introduction. A non-toxic and stable sarin analogue, isopropyl p-nitrophenyl methylphosphonate (INMP), was synthesized for safe preparation of sarin-exposed acetylcholinesterase (AChE). Results and Discussion. This agent was stable for years, able to be handled in an ordinary laboratory without special care, and its 50% inhibitory concentration (IC50) on 0.04 U/ml human erythrocytes AChE was 15 nM. This reagent was thought to be especially useful since it enables experiments that require sarin-inhibited AChE, such as the development of antidotes for sarin, in a usual laboratory. To demonstrate the usefulness of this method, 40 known and novel pyridinealdoxime methiodide (PAM)-type oxime antidotes were synthesized, and their reactivation activities to INMP-exposed AChE and structure-activities correlation were studied. Conclusion. Among the antidotes tested in this experiment except for 2-PAM, the compound found to have the highest reactivation activity, was the novel hydrophobic 2-PAM-type compound, 2-[(hydroxyimino)methyl]-1-[4-(tert- butyl)benzyl] pyridinium bromide.
