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116797-02-5

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116797-02-5 Usage

General Description

4-Methyl-[1,4']bipiperidinyl is a chemical compound belonging to the class of bipiperidine derivatives. It is a heterocyclic compound with a molecular formula of C11H22N2 and a molecular weight of 174.3 g/mol. 4-METHYL-[1,4']BIPIPERIDINYL has two piperidine rings connected by a methylene bridge, and a methyl substituent at the 4-position of one of the piperidine rings. 4-Methyl-[1,4']bipiperidinyl is used in the development of various pharmaceuticals and can act as a precursor in the synthesis of other complex organic compounds. Its specific properties and applications may vary depending on the context and the chemical reactions involved.

Check Digit Verification of cas no

The CAS Registry Mumber 116797-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,7,9 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116797-02:
(8*1)+(7*1)+(6*6)+(5*7)+(4*9)+(3*7)+(2*0)+(1*2)=145
145 % 10 = 5
So 116797-02-5 is a valid CAS Registry Number.

116797-02-5SDS

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 4-methyl-1-piperidin-4-ylpiperidine

1.2 Other means of identification

Product number -
Other names 4-methyl-1-(4-piperidyl)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:116797-02-5 SDS

116797-02-5Downstream Products

116797-02-5Relevant articles and documents

Synthesis and conformational study of water-soluble, rigid, rodlike oligopiperidines

Semetey, Vincent,Moustakas, Demetri,Whitesides, George M.

, p. 588 - 591 (2007/10/03)

An oligomeric backbone of piperidine rings can be synthesized by solution or solid-phase synthesis. These oligomers adopt well-defined, rodlike structures with all the piperidine residues in chair conformations (see picture) both in solution (D2O, CD3OD) and the solid state. (Figure Presented).

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