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(R)-1-methoxypropan-2-amine hydrochloride, also known as Methoxyphenidine, is a research chemical with psychoactive properties. It belongs to the arylcyclohexylamine class of drugs and is structurally similar to dissociative anesthetics such as phencyclidine (PCP) and ketamine. (R)-1-methoxypropan-2-amine hydrochloride is known for its ability to induce dissociation, hallucinations, and euphoria, and is primarily used for research purposes to explore its potential in treating various psychological conditions.

626220-76-6

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626220-76-6 Usage

Uses

Used in Pharmaceutical Research:
(R)-1-methoxypropan-2-amine hydrochloride is used as a research chemical for investigating its potential therapeutic applications in treating psychological conditions. Its psychoactive properties, including dissociation, hallucinations, and euphoria, make it a valuable tool for studying the underlying mechanisms of these conditions and developing novel treatment strategies.
Used in Drug Development:
In the pharmaceutical industry, (R)-1-methoxypropan-2-amine hydrochloride is used as a lead compound in the development of new drugs targeting specific psychological disorders. Its structural similarity to other dissociative anesthetics allows researchers to explore its potential as a therapeutic agent, with the aim of improving the safety and efficacy of existing treatments.
Used in Neuroscientific Research:
(R)-1-methoxypropan-2-amine hydrochloride is employed as a research tool in neuroscientific studies to better understand the neural mechanisms underlying the psychoactive effects of arylcyclohexylamine drugs. By examining the interactions of (R)-1-methoxypropan-2-amine hydrochloride with various neurotransmitter systems, researchers can gain insights into the pathways involved in dissociation, hallucinations, and euphoria, potentially leading to the discovery of new therapeutic targets.
Used in Toxicological Studies:
In toxicology, (R)-1-methoxypropan-2-amine hydrochloride is used to evaluate the safety and potential side effects of this class of drugs. By studying its pharmacokinetics, metabolism, and toxicological profile, researchers can assess the risks associated with its use and develop strategies to mitigate any adverse effects.
Used in Forensic Analysis:
(R)-1-methoxypropan-2-amine hydrochloride is utilized in forensic analysis to detect and identify the presence of this psychoactive substance in biological samples, such as blood or urine. This is crucial for legal purposes, particularly in cases involving drug abuse or intoxication-related incidents.

Check Digit Verification of cas no

The CAS Registry Mumber 626220-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,6,2,2 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 626220-76:
(8*6)+(7*2)+(6*6)+(5*2)+(4*2)+(3*0)+(2*7)+(1*6)=136
136 % 10 = 6
So 626220-76-6 is a valid CAS Registry Number.

626220-76-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-Methoxypropan-2-amine hydrochloride

1.2 Other means of identification

Product number -
Other names (2R)-1-methoxypropan-2-amine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:626220-76-6 SDS

626220-76-6Relevant academic research and scientific papers

THIAZOLE AND OXAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

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Page/Page column 36, (2012/02/03)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is a group of formula A or formula B, and X, R2, R3, R4, R5, R6, Ra and Rb are as defined herein. Also provided are methods of using the compounds for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist and methods of making the subject compounds.

ISOINDOLYL COMPOUNDS

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Page/Page column 27-28, (2012/06/30)

Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein the variables are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with the P2X7 purinergic receptor

BIPHENYL AND PHENYL-PYRIDINE AMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

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Page/Page column 30, (2010/12/31)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted phenyl or optionally substituted pyridinyl, and R2, R3, R4, R5, R6, R7, R8 and R9 are as defined herein. Also disclosed are methods of using the compounds for treating diseases associated with P2X3 and/or a P2X2/3 receptor antagonists and methods of making the compounds.

Tetrazole-substituted arylamides as P2X3 and P2X2/3 antagonists

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Page/Page column 40, (2009/07/10)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted tetrazolyl, R2 is optionally substituted phenyl, optionally substituted pyridinyl or optionally substituted thienyl, and R3, R4, R5, R6 R7 and R8 are as defined herein. Also provided are methods of using the compounds for treating diseases associated with the P2X3 and/or a P2X2/3 receptor antagonist and methods of making the compounds.

Imidazole-substituted arylamides as P2X3 and P2X2/3 antagonists

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Page/Page column 28, (2009/07/10)

Compounds of the formula I: wherein R1 is optionally substituted imidazolyl, and R2, R3, R4, R5, R6, R7 and R8 are as defined herein. Also provided are methods of using the compounds for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist and methods of making the subject compounds.

Tetrazole-substituted arylamides as P2X3 and P2X2/3 antagonists

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Page/Page column 197, (2008/06/13)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is optionally substituted tetrazolyl, R2 is optionally substituted phenyl, optionally substituted pyridinyl or optionally substituted thienyl, and R3, R4, R5 and R6 are as defined herein. Also provided are methods of using the compounds for treating diseases associated with the P2X3 and/or a P2X2/3 receptor antagonist and methods of making the compounds.

THIAZOLE AND OXAZOLE-SUBSTITUTED ARYLAMIDES

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Page/Page column 58, (2008/12/05)

Compounds of the formula (I) or a pharmaceutically acceptable salt thereof, wherein: R1 is a group of formula A or formula B; and X, R2, R3, R4, R5, R6, Ra and Rb are as defined herein. Also provided are methods of using the compounds for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist and methods of making the subject compounds.

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