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CAS

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136422-65-6

3-(4-Methoxy-benzyl)-piperidine is a chemical compound that belongs to the class of organic compounds known as benzene and substituted derivatives. It is an aromatic compound containing a monocyclic ring system made of six carbon atoms and benzene, with a six-membered piperidine ring attached to the benzyl portion. The 4-methoxy-benzyl group is a benzyl group substituted at the fourth position by a methoxy group, which is the simplest ether constituent. 3-(4-METHOXY-BENZYL)-PIPERIDINE is recognized for its functional group reactivity and ring structure, and its properties may vary based on its specific use, concentration, or modification in chemical reactions.

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  • 136422-65-6 Structure

  • Basic information

    1. Product Name: 3-(4-METHOXY-BENZYL)-PIPERIDINE
    2. Synonyms: 3-(4-METHOXY-BENZYL)-PIPERIDINE;3-[(4-METHOXYPHENYL)METHYL]-PIPERIDINE;OTAVA-BB 1043239
    3. CAS NO:136422-65-6
    4. Molecular Formula: C13H19NO
    5. Molecular Weight: 205.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136422-65-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 315°C at 760 mmHg
    3. Flash Point: 129.4°C
    4. Appearance: /
    5. Density: 1.002g/cm3
    6. Vapor Pressure: 0.000449mmHg at 25°C
    7. Refractive Index: 1.519
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 10.30±0.10(Predicted)
    11. CAS DataBase Reference: 3-(4-METHOXY-BENZYL)-PIPERIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-(4-METHOXY-BENZYL)-PIPERIDINE(136422-65-6)
    13. EPA Substance Registry System: 3-(4-METHOXY-BENZYL)-PIPERIDINE(136422-65-6)

  • 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: 136422-65-6(Hazardous Substances Data)

136422-65-6 Usage

Uses

Used in Pharmaceutical Chemistry:
3-(4-Methoxy-benzyl)-piperidine is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its functional group reactivity and ring structure make it a valuable building block in the synthesis of new drugs.
Used in Chemical Research:
3-(4-Methoxy-benzyl)-piperidine is used as a research compound in the field of organic chemistry. Its unique structure and properties allow chemists to study its reactivity and potential applications in various chemical reactions and processes.
Used in Material Science:
3-(4-Methoxy-benzyl)-piperidine may be used as a component in the development of new materials with specific properties, such as improved stability or reactivity, due to its aromatic and amine-containing structure.

Check Digit Verification of cas no

The CAS Registry Mumber 136422-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,2 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136422-65:
(8*1)+(7*3)+(6*6)+(5*4)+(4*2)+(3*2)+(2*6)+(1*5)=116
116 % 10 = 6
So 136422-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO/c1-15-13-6-4-11(5-7-13)9-12-3-2-8-14-10-12/h4-7,12,14H,2-3,8-10H2,1H3

136422-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-methoxyphenyl)methyl]piperidine

1.2 Other means of identification

Product number -
Other names BP038

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:136422-65-6 SDS

136422-65-6Relevant articles and documents

A facile synthesis of 3-(substituted benzyl)piperidines

ágai, Béla,Nádor, Adrienn,Proszenyák, ágnes,Tárkányi, Gábor,Faigl, Ferenc

, p. 7897 - 7900 (2007/10/03)

A convenient new method has been developed for preparation a series of 3-(substituted benzyl)piperidines by addition of substituted phenylmagnesium bromide to pyridine-3-carboxaldehyde followed by one pot deoxygenation and heteroaromatic ring saturation in the presence of palladium catalyst.

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