O-2482 is , while it's Molecular Formula is C 19 H 23 NO. Used in Pharmaceutical Research: O-2482 is used as a research compound for understanding the mechanisms of opioid receptors and developing new therapeutic agents with reduced risks of addiction and overdose. Its potent agonist activity provides valuable insights into the development of safer opioid medications. Used in Forensic Toxicology: O-2482 is utilized as a target analyte in forensic toxicology for the detection and analysis of synthetic opioid abuse and overdose cases. Its identification in biological samples helps in determining the cause of death and understanding the extent of synthetic opioid misuse in the population. Used in Public Health Policy and Regulation: O-2482 serves as a reference substance in the development of public health policies and regulatory measures aimed at controlling the availability and distribution of synthetic opioids. Its classification as a controlled substance helps in monitoring and preventing the misuse and abuse of these potent chemicals. Used in Drug Rehabilitation Programs: O-2482 is employed as an educational tool in drug rehabilitation programs to raise awareness about the dangers of synthetic opioid use and the risks associated with addiction and overdose. Its potent effects on the central nervous system highlight the importance of proper treatment and support for individuals struggling with opioid dependence.

What is the CAS number for O-2482?

The CAS number of O-2482 is 850352-53-3.

What is O-2482 (850352-53-3) used for?

O-2482 is a class of synthetic opioids structurally related to fentanyl and its analogs. As potent opioid receptor agonists, they exert a powerful effect on the central nervous system, leading to a high risk of overdose and death. Due to their association with illicit drug use and potential for abuse and addiction, O-2482 and its analogs have become a subject of concern for public health officials. Consequently, these chemicals have been classified as controlled substances and are regulated by legal authorities to reduce their availability and prevent misuse.InChI:InChI=1/C19H23NO/c1-2-7-18(20-12-5-6-13-20)19(21)17-11-10-15-8-3-4-9-16(15)14-17/h3-4,8-11,14,18H,2,5-7,12-13H2,1H3

O-2482 is , while it's Molecular Formula is C 19 H 23 NO. Used in Pharmaceutical Research: O-2482 is used as a research compound for understanding the mechanisms of opioid receptors and developing new therapeutic agents with reduced risks of addiction and overdose. Its potent agonist activity provides valuable insights into the development of safer opioid medications. Used in Forensic Toxicology: O-2482 is utilized as a target analyte in forensic toxicology for the detection and analysis of synthetic opioid abuse and overdose cases. Its identification in biological samples helps in determining the cause of death and understanding the extent of synthetic opioid misuse in the population. Used in Public Health Policy and Regulation: O-2482 serves as a reference substance in the development of public health policies and regulatory measures aimed at controlling the availability and distribution of synthetic opioids. Its classification as a controlled substance helps in monitoring and preventing the misuse and abuse of these potent chemicals. Used in Drug Rehabilitation Programs: O-2482 is employed as an educational tool in drug rehabilitation programs to raise awareness about the dangers of synthetic opioid use and the risks associated with addiction and overdose. Its potent effects on the central nervous system highlight the importance of proper treatment and support for individuals struggling with opioid dependence.

What is the CAS number for O-2482?

The CAS number of O-2482 is 850352-53-3.

What is O-2482 (850352-53-3) used for?

O-2482 is a class of synthetic opioids structurally related to fentanyl and its analogs. As potent opioid receptor agonists, they exert a powerful effect on the central nervous system, leading to a high risk of overdose and death. Due to their association with illicit drug use and potential for abuse and addiction, O-2482 and its analogs have become a subject of concern for public health officials. Consequently, these chemicals have been classified as controlled substances and are regulated by legal authorities to reduce their availability and prevent misuse.InChI:InChI=1/C19H23NO/c1-2-7-18(20-12-5-6-13-20)19(21)17-11-10-15-8-3-4-9-16(15)14-17/h3-4,8-11,14,18H,2,5-7,12-13H2,1H3

O-2482

CAS：850352-53-3
MF：C₁₉H₂₃NO
Purity：99%
Molecular Weight：281.398

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Product Details

CAS： 850352-53-3

MF： C₁₉H₂₃NO

Chinese Manufacturer Supply O-2482 850352-53-3 On Stock with Competitive Price

Molecular Formula:C₁₉H₂₃NO
Molecular Weight:281.398
Vapor Pressure:1.29E-07mmHg at 25°C
Refractive Index:1.596
Boiling Point:430.5°C at 760 mmHg
Flash Point:161.4°C
PSA：20.31000
Density:1.088g/cm³
LogP:4.22490

O-2482(Cas 850352-53-3) Usage

General Description

O-2482 refers to a class of synthetic opioids that are structurally related to fentanyl and its analogs. These chemicals are potent opioid receptor agonists and have been associated with a high risk of overdose and death due to their powerful effect on the central nervous system. O-2482 and its analogs have been implicated in numerous cases of illicit drug use and have been the subject of concern for public health officials due to their potential for abuse and addiction. These chemicals have been classified as controlled substances and are regulated by legal authorities in an effort to reduce their availability and prevent their misuse.

InChI:InChI=1/C19H23NO/c1-2-7-18(20-12-5-6-13-20)19(21)17-11-10-15-8-3-4-9-16(15)14-17/h3-4,8-11,14,18H,2,5-7,12-13H2,1H3

850352-53-3 Relevant articles

1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (pyrovalerone) analogues: A promising class of monoamine uptake inhibitors

Meltzer, Peter C.,Butler, David,Deschamps, Jeffrey R.,Madras, Bertha K.

, p. 1420 - 1432 (2006)

Dopamine, serotonin, and norepinephrine ...

850352-53-3 Process route

: 613-46-7
2-naphthalenecarbonitrile

: 850352-53-3
naphyrone

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: toluene 1.2: aq. H₂SO₄ / toluene 2.1: AlCl₃; bromine 3.1: diethyl ether / 22 °C With aluminium trichloride; bromine; In diethyl ether; toluene;

: 33489-63-3
1-naphthalen-2-yl-pentan-1-one

: 850352-53-3
naphyrone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: AlCl₃; bromine 2: diethyl ether / 22 °C With aluminium trichloride; bromine; In diethyl ether;

850352-53-3 Upstream products

123-75-1
pyrrolidine
850352-43-1
2-bromo-1-naphthalen-2-yl-pentan-1-one
613-46-7
2-naphthalenecarbonitrile
33489-63-3
1-naphthalen-2-yl-pentan-1-one

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