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CAS

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215183-32-7

(S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one, commonly known as R-phenibut, is a chemical compound with psychoactive properties. It is a derivative of the neurotransmitter GABA (gamma-aminobutyric acid) and is recognized for its potential to reduce anxiety, improve cognitive function, and enhance mood. However, it can also have sedative effects and may lead to dependence and withdrawal symptoms with long-term use. Due to its psychoactive properties, R-phenibut is regulated in some countries and may require a prescription or be prohibited for use without medical supervision.

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  • 215183-32-7 Structure

  • Basic information

    1. Product Name: (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one
    2. Synonyms: (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one
    3. CAS NO:215183-32-7
    4. Molecular Formula: C13H17NO2
    5. Molecular Weight: 219.27958
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 215183-32-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one(215183-32-7)
    11. EPA Substance Registry System: (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one(215183-32-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 215183-32-7(Hazardous Substances Data)

215183-32-7 Usage

Uses

Used in Pharmaceutical Applications:
(S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one is used as a nootropic for enhancing cognitive function, as it is believed to improve brain function and mental clarity.
Used in Anxiolytic Applications:
(S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one is used as an anxiolytic to help reduce anxiety and promote a sense of calm and relaxation.
Used in Sedative Applications:
(S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one is used as a sedative to induce sleep and help with insomnia.
Used in Recreational Applications:
(S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one is used recreationally for its mood-enhancing and relaxing effects, although it carries a moderate risk of abuse and is regulated in some countries.
Used in Medical Supervision:
Due to its potential for dependence and withdrawal symptoms, (S)-4-(hydroxyMethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one is used under medical supervision in some countries, where it may require a prescription for safe and controlled use.

Check Digit Verification of cas no

The CAS Registry Mumber 215183-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,1,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 215183-32:
(8*2)+(7*1)+(6*5)+(5*1)+(4*8)+(3*3)+(2*3)+(1*2)=107
107 % 10 = 7
So 215183-32-7 is a valid CAS Registry Number.

215183-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-4-(hydroxymethyl)-1-[(1R)-phenylethyl]pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names (S)-4-(Hydroxymethyl)-1-((R)-1-phenylethyl)pyrrolidin-2-one

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:215183-32-7 SDS

215183-32-7Relevant articles and documents

New chiral 3-naphthylaminomethylpyrrolidines: An unexpected epimerisation reaction

Fava, Cristiana,Galeazzi, Roberta,Mobbili, Giovanna,Orena, Mario

, p. 2463 - 2470 (2007/10/03)

New enantiomerically pure 3-naphthylaminomethylpyrrolidines (8), (9), (14) and (15) were obtained through simple steps starting from chiral 4- ethenylpyrrolidin-2-ones (2) and (3). On the other hand, starting from pyrrolidine (16), an epimerisation reacti

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