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CAS

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27393-78-8

(1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE, also known as ALD-52, is a chemical compound that belongs to the class of indole alkaloids. It is a derivative of LSD and is classified as a psychedelic drug. ALD-52 is known for its hallucinogenic properties and is often used recreationally for its mind-altering effects. It is also being studied for its potential therapeutic applications in treating mental health disorders, such as depression and anxiety. However, its use is regulated in many countries due to its psychoactive nature and potential for abuse.

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  • 27393-78-8 Structure

  • Basic information

    1. Product Name: (1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE
    2. Synonyms: 1H-INDOL-3-YL(1-PYRROLIDINYL)METHANONE;(1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE;3-(pyrrolidine-1-carbonyl)-1H-indole
    3. CAS NO:27393-78-8
    4. Molecular Formula: C13H14N2O
    5. Molecular Weight: 214.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27393-78-8.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: (1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE(27393-78-8)
    11. EPA Substance Registry System: (1H-INDOL-3-YL)(PYRROLIDIN-1-YL)METHANONE(27393-78-8)

  • 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: 27393-78-8(Hazardous Substances Data)

27393-78-8 Usage

Uses

Used in Pharmaceutical Industry:
ALD-52 is used as a research chemical for studying the effects of psychedelic drugs on the human brain. Its hallucinogenic properties make it a valuable tool in understanding the neural mechanisms underlying perception, cognition, and emotion.
Used in Mental Health Treatment:
ALD-52 is being studied for its potential therapeutic applications in treating mental health disorders, such as depression and anxiety. Its mind-altering effects may help patients gain new insights and perspectives on their mental health issues, leading to improved treatment outcomes.
Used in Recreational Settings:
ALD-52 is used recreationally for its hallucinogenic properties, providing users with altered perceptions, enhanced sensory experiences, and profound psychological effects. However, its use in this context is regulated due to its psychoactive nature and potential for abuse.

Check Digit Verification of cas no

The CAS Registry Mumber 27393-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,9 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27393-78:
(7*2)+(6*7)+(5*3)+(4*9)+(3*3)+(2*7)+(1*8)=138
138 % 10 = 8
So 27393-78-8 is a valid CAS Registry Number.

27393-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(indole-3-carbonyl)-pyrrolidine

1.2 Other means of identification

Product number -
Other names -

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:27393-78-8 SDS

27393-78-8Downstream Products

27393-78-8Relevant articles and documents

Synthesis method of 6-hydroisoindolo[2,1-alpha]indole compounds

-

Paragraph 0031-0032; 0049-0053, (2021/07/14)

The invention relates to a synthesis method of 6-hydroisoindolo[2,1-alpha]indole compounds, wherein the synthesis method comprises the steps: in an organic solvent system, synthesizing by taking a 1-aryl methylene indole compound as a basic raw material i

A practical synthesis of indole-based heterocycles using an amidoaluminum-mediated strategy

Todd, Robert,Hossain, M. Mahmun

experimental part, p. 1846 - 1850 (2010/01/16)

A large number of biologically active compounds consist of an indole scaffolding. Because of this, chemists are continually searching for more efficient means through which to successfully synthesize the required alkaloids. In our recent effort to synthes

Synthesis of indole-3-carboxamides via a haloform cleavage reaction of 3-trifluoroacetylindole with lithium dialkylamides

Hassinger, Heidi L.,Soll, Richard M.,Gribble, Gordon W.

, p. 3095 - 3098 (2007/10/03)

Reaction of 3-trifluoroacetylindole (4) with lithium dialkylamides affords the corresponding indole-3-carboxamides (5) in good to excellent yields.

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