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2961-47-9

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2961-47-9 Usage

General Description

4-(5-Nonyl)pyridine is a chemical compound with the molecular formula C16H27N. It is a pyridine derivative that consists of a pyridine ring substituted with a nonyl group at the 4-position. 4-(5-NONYL)PYRIDINE is known for its use as a building block in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. It has also been studied for its potential use in the development of new materials, such as polymers and surfactants. 4-(5-Nonyl)pyridine is considered to be a hazardous chemical and should be handled with care due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 2961-47-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2961-47:
(6*2)+(5*9)+(4*6)+(3*1)+(2*4)+(1*7)=99
99 % 10 = 9
So 2961-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H23N/c1-3-5-7-13(8-6-4-2)14-9-11-15-12-10-14/h9-13H,3-8H2,1-2H3

2961-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nonan-5-ylpyridine

1.2 Other means of identification

Product number -
Other names 5-(4-Pyridyl)nonane

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:2961-47-9 SDS

2961-47-9Relevant articles and documents

BIS-PYRIDINIUM COMPOUNDS

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Page/Page column 25, (2008/06/13)

A method of treating, inhibiting, or preventing an infection in a subject is described. The method comprises administering to the subject an effective amount of at least one bis-pyridinium compound. The bis-pyridinium compound comprises two aromatic ring structures. Each of the ring structures comprises a pyridine ring, and the ring structures are linked by a linker group of at least 8 atoms in length, said linker group being attached to the nitrogen atoms of the pyridine rings. At least one substituent on at least one of the ring structures is an alkyl group having at least 2 carbon atoms, and no substituent on either of the ring structures is -OH, -SH or an amine group.

Substituted 2,2'-bipyridyl compounds and process for preparing same

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, (2008/06/13)

A process for preparing substituted 2,2'-bipyridyl compounds and several compounds so prepared, the process comprising the steps of first selecting a substituted pyridine of the formula defined herein, then mixing a stoichiometric excess of the substituted pyridine with an amount of sodamide, causing the resultant mixture to be at a temperature sufficiently high to cause substituted 2,2'-bipyridyl formation, and isolating the substituted 2,2'-bipyridyl thereby formed. The new substituted 2,2'-bipyridyl compounds are selected from the group consisting of 4,4'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(cyclohexylmethyl)-2,2'-bipyridyl; 5,5'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-phenylpropyl)-2,2'-bipyridyl; 4,4'-di-(4-tetrahydropyranyl)-2,2'-bipyridyl; 4,4'-di-benzyl-2,2'-bipyridyl; 6,6'-di-isoamyl-2,2'-bipyridyl; and 4,4'-di-(t-butyl)-2,2'-bipyridyl.

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