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104-89-2

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104-89-2 Usage

General Description

5-ETHYL-2-METHYLPIPERIDINE is a heterocyclic compound with a piperidine ring structure and substituent groups of ethyl and methyl. It is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of other organic compounds. This chemical has potential applications in the development of medications for conditions such as depression, anxiety, and Parkinson's disease. Additionally, it may also have uses in the field of organic chemistry as a building block for the creation of more complex molecules. However, it is important to handle 5-ETHYL-2-METHYLPIPERIDINE with caution and follow proper safety protocols due to its potential hazards as a chemical substance.

Check Digit Verification of cas no

The CAS Registry Mumber 104-89-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104-89:
(5*1)+(4*0)+(3*4)+(2*8)+(1*9)=42
42 % 10 = 2
So 104-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H17N/c1-3-8-5-4-7(2)9-6-8/h7-9H,3-6H2,1-2H3/t7-,8+/m0/s1

104-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ETHYL-2-METHYLPIPERIDINE

1.2 Other means of identification

Product number -
Other names 5-ethyl-2-methyl-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:104-89-2 SDS

104-89-2Relevant articles and documents

Process for increasing the cis content of a mixture of cis and trans isomers of S-isopropyl-1-(5-ethyl-2-methylpiperidinecarbothioate)

-

, (2008/06/13)

A mixture of cis and trans isomers of S-isopropyl-1-(5-ethyl-2-methylpiperidinecarbothioate) has been found to have improved herbicidal properties in contrast to the trans isomer alone. Preferably the mixture contains at least about 20%, most preferably between about 60 and about 65%, of the cis isomer. The S-isopropyl-1-(5-ethyl-2-methylpiperidinecarbothioate) having a desired amount of cis isomer can be produced by a two-step process comprising hydrogenation of 2-methyl-5-ethyl pyridine using a catalyst comprising rhodium supported on activated carbon to produce 2-methyl-5-ethyl piperidine and reacting the piperidine with isopropyl chlorothiolformate.

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