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5608-82-2

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5608-82-2 Usage

General Description

4,4-dimethoxypiperidine is a chemical compound with the molecular formula C7H15NO2. It is a piperidine derivative with two methoxy groups attached at the 4 position of the piperidine ring. 4,4-dimethoxypiperidine is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and organic compounds. It has been found to have potential antibacterial, antifungal, and antiviral properties, and is being studied for its potential as a therapeutic agent. 4,4-dimethoxypiperidine is a colorless liquid with a slightly sweet odor, and it is soluble in organic solvents such as ethanol and ether. Due to its reactivity and potential health hazards, proper handling and safety precautions are recommended when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 5608-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5608-82:
(6*5)+(5*6)+(4*0)+(3*8)+(2*8)+(1*2)=102
102 % 10 = 2
So 5608-82-2 is a valid CAS Registry Number.

5608-82-2SDS

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 4,4-dimethoxypiperidine

1.2 Other means of identification

Product number -
Other names 4,4-dimethoxy-piperidine

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:5608-82-2 SDS

5608-82-2Relevant articles and documents

Radical reductive alkylation of enamines: Conversion of the products into alkenes and primary amines

Renaud,Betrisey

, p. 3479 - 3491 (2007/10/03)

Procedures for the conversion of tertiary amines, obtained by radical reductive alkylation of enamines, into alkenes (Cope reaction) and primary amines (double β-elimination reaction) are presented.

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