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41447-15-8

(-)-N-Methylsedridine is a heterocyclic compound characterized by a 1-methylpiperidine ring. As a chiral molecule, it exhibits two enantiomers and is naturally present in certain plants and fruits. Its pharmacological properties have been of interest due to its potential as a ligand for the α7 nicotinic acetylcholine receptor, which suggests its utility in addressing neurological and psychiatric disorders. Additionally, (-)-N-Methylsedridine has demonstrated insecticidal and anti-microbial activities, positioning it as a promising candidate for the creation of innovative agricultural and pharmaceutical products.

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  • 41447-15-8 Structure

  • Basic information

    1. Product Name: (-)-N-Methylsedridine
    2. Synonyms: (-)-N-Methylsedridine
    3. CAS NO:41447-15-8
    4. Molecular Formula: C9H19NO
    5. Molecular Weight: 157.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41447-15-8.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: (-)-N-Methylsedridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-N-Methylsedridine(41447-15-8)
    11. EPA Substance Registry System: (-)-N-Methylsedridine(41447-15-8)

  • 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: 41447-15-8(Hazardous Substances Data)

41447-15-8 Usage

Uses

Used in Pharmaceutical Development:
(-)-N-Methylsedridine is used as a pharmacological agent for its potential role in treating neurological and psychiatric disorders. Its interaction with the α7 nicotinic acetylcholine receptor makes it a candidate for further research and development in this therapeutic area.
Used in Agricultural Applications:
(-)-N-Methylsedridine is used as an insecticide and anti-microbial agent in agriculture. Its natural insecticidal and anti-microbial properties suggest its potential use in developing new pest control methods and products, contributing to more sustainable and effective agricultural practices.
Used in Chemical Research:
(-)-N-Methylsedridine serves as a subject of study in chemical research, particularly in the exploration of chiral molecules and their synthesis, as well as their applications in various fields such as medicine and agriculture. Its unique properties and natural occurrence make it an intriguing compound for scientific investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 41447-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41447-15:
(7*4)+(6*1)+(5*4)+(4*4)+(3*7)+(2*1)+(1*5)=98
98 % 10 = 8
So 41447-15-8 is a valid CAS Registry Number.

41447-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[(2S)-1-Methyl-2-piperidinyl]-2-propanol

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:41447-15-8 SDS

41447-15-8Downstream Products

41447-15-8Relevant articles and documents

Synthesis of bicyclic carbamates as precursors of Sedum alkaloid derivatives

Szakonyi, Zsolt,D'Hooghe, Matthias,Kanizsai, Iván,Fül?p, Ferenc,De Kimpe, Norbert

, p. 1595 - 1602 (2007/10/03)

Synthesis of a N-Boc-protected piperidin-2-yl phosphine oxide starting from piperidine in three steps, followed by olefination using a variety of α,β-unsaturated aldehydes resulted in tert-butyl 2-(2′- alkenylidene)piperidine-1-carboxylates in high yields

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