What is the Cumyl-PINACA?

Cumyl-PINACA is , while it's Molecular Formula is C 22 H 27 N 3 O. Used in Pharmaceutical Research: Cumyl-PINACA is used as a research chemical for studying the effects and mechanisms of action at the CB1 and CB2 receptors. Its potent agonist activity allows scientists to investigate the therapeutic potential of targeting these receptors for various medical conditions. Used in Toxicological Studies: Due to its classification as a Schedule I controlled substance and its association with adverse health effects, Cumyl-PINACA is used in toxicological studies to understand the risks and consequences of synthetic cannabinoid abuse. This research aids in the development of strategies for prevention, intervention, and treatment of synthetic cannabinoid-related health issues. Used in Forensic Analysis: Cumyl-PINACA is utilized in forensic analysis to detect and identify the presence of this synthetic cannabinoid in samples related to drug abuse cases. This helps in the enforcement of laws and regulations against the production, distribution, and use of synthetic cannabinoids. Used in Drug Policy and Regulation Development: The presence of Cumyl-PINACA in synthetic cannabis products and its potential for abuse and harm has led to its inclusion in discussions and policies related to drug regulation. It serves as a case study for the development of guidelines and regulations to control the circulation of synthetic cannabinoids and protect public health.

What is the CAS number for Cumyl-PINACA?

The CAS number of Cumyl-PINACA is 1400742-15-5.

What is Cumyl-PINACA (1400742-15-5) used for?

Cumyl-PINACA, also known as SGT-24, is a synthetic cannabinoid that functions as a potent agonist at the CB1 and CB2 receptors. Initially identified in Japan in 2013, it has been recognized as a component in synthetic cannabis products. Due to its association with severe adverse effects such as seizures, psychosis, and even fatalities, it has been categorized as a Schedule I controlled substance in the United States and prohibited in numerous countries. The chemical structure of Cumyl-PINACA features a cumyl group, which is prevalent among synthetic cannabinoids and is often utilized to substitute the more traditional JWH groups in these compounds.

What is the Cumyl-PINACA?

Cumyl-PINACA is , while it's Molecular Formula is C 22 H 27 N 3 O. Used in Pharmaceutical Research: Cumyl-PINACA is used as a research chemical for studying the effects and mechanisms of action at the CB1 and CB2 receptors. Its potent agonist activity allows scientists to investigate the therapeutic potential of targeting these receptors for various medical conditions. Used in Toxicological Studies: Due to its classification as a Schedule I controlled substance and its association with adverse health effects, Cumyl-PINACA is used in toxicological studies to understand the risks and consequences of synthetic cannabinoid abuse. This research aids in the development of strategies for prevention, intervention, and treatment of synthetic cannabinoid-related health issues. Used in Forensic Analysis: Cumyl-PINACA is utilized in forensic analysis to detect and identify the presence of this synthetic cannabinoid in samples related to drug abuse cases. This helps in the enforcement of laws and regulations against the production, distribution, and use of synthetic cannabinoids. Used in Drug Policy and Regulation Development: The presence of Cumyl-PINACA in synthetic cannabis products and its potential for abuse and harm has led to its inclusion in discussions and policies related to drug regulation. It serves as a case study for the development of guidelines and regulations to control the circulation of synthetic cannabinoids and protect public health.

What is the CAS number for Cumyl-PINACA?

The CAS number of Cumyl-PINACA is 1400742-15-5.

What is Cumyl-PINACA (1400742-15-5) used for?

Cumyl-PINACA, also known as SGT-24, is a synthetic cannabinoid that functions as a potent agonist at the CB1 and CB2 receptors. Initially identified in Japan in 2013, it has been recognized as a component in synthetic cannabis products. Due to its association with severe adverse effects such as seizures, psychosis, and even fatalities, it has been categorized as a Schedule I controlled substance in the United States and prohibited in numerous countries. The chemical structure of Cumyl-PINACA features a cumyl group, which is prevalent among synthetic cannabinoids and is often utilized to substitute the more traditional JWH groups in these compounds.

Product

Current location：Home > Product > Cumyl-PINACA

Cumyl-PINACA

Name Cumyl-PINACA
CAS 1400742-15-5
Purity 99%

Inquiry

Product Details

Perfect Factory Offer Excellent quality Cumyl-PINACA 1400742-15-5 with Safe Shipping

Molecular Formula: C₂₂H₂₇N₃O
Molecular Weight: 349.476

1400742-15-5 Relevant articles

Pharmacology of Cumyl-Carboxamide Synthetic Cannabinoid New Psychoactive Substances (NPS) CUMYL-BICA, CUMYL-PICA, CUMYL-5F-PICA, CUMYL-5F-PINACA, and Their Analogues

Longworth, Mitchell,Banister, Samuel D.,Boyd, Rochelle,Kevin, Richard C.,Connor, Mark,McGregor, Iain S.,Kassiou, Michael

, p. 2159 - 2167 (2017/10/23)

Synthetic cannabinoids (SC) are the larg...

CANNABINOID COMPOUNDS

-

Page/Page column 102, (2014/10/29)

The present invention relates generally ...

1400742-15-5 Process route

: 1-pentyl-1H-indazole-3-carboxylic acid

: 585-32-0
2-phenyl-2-propylamine

: 1400742-15-5
Cumyl-PINACA

Conditions

Conditions	Yield
1-pentyl-1H-indazole-3-carboxylic acid; With oxalyl dichloride; In dichloromethane; at 0 ℃; for 0.5h; 2-phenyl-2-propylamine; With triethylamine; In dichloromethane; for 1h;	78%
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; at 20 ℃; for 14h; Inert atmosphere;

: 942-24-5
3-methoxycarbonylindole

: 1400742-15-5
Cumyl-PINACA

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: potassium tert -butylate / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere 1.2: 48 h / 0 °C 2.1: sodium hydroxide; water / methanol / 18 h / Reflux; Inert atmosphere 3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 14 h / 20 °C / Inert atmosphere With potassium tert-butylate; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; dimethyl sulfoxide;

Yield

Multi-step reaction with 3 steps

1.1: potassium tert -butylate / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

1.2: 48 h / 0 °C

2.1: sodium hydroxide; water / methanol / 18 h / Reflux; Inert atmosphere

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 14 h / 20 °C / Inert atmosphere

With potassium tert-butylate; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; dimethyl sulfoxide;

1400742-15-5 Upstream products

585-32-0
2-phenyl-2-propylamine
942-24-5
3-methoxycarbonylindole

Home

Company Introduction

Product

Pharmaceutical

Others

Industry News

Contact Information

Product

Cumyl-PINACA

Perfect Factory Offer Excellent quality Cumyl-PINACA 1400742-15-5 with Safe Shipping

1400742-15-5 Relevant articles

Pharmacology of Cumyl-Carboxamide Synthetic Cannabinoid New Psychoactive Substances (NPS) CUMYL-BICA, CUMYL-PICA, CUMYL-5F-PICA, CUMYL-5F-PINACA, and Their Analogues

Longworth, Mitchell,Banister, Samuel D.,Boyd, Rochelle,Kevin, Richard C.,Connor, Mark,McGregor, Iain S.,Kassiou, Michael

, p. 2159 - 2167 (2017/10/23)

CANNABINOID COMPOUNDS

-

Page/Page column 102, (2014/10/29)

1400742-15-5 Process route

1400742-15-5 Upstream products

Related products