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70525-40-5

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70525-40-5 Usage

General Description

2-(cyclohexylidenemethyl)pyridine, also known as CMP, is an organic compound with the molecular formula C13H15N. It is a pyridine derivative that contains a cyclohexyl group attached to the pyridine ring through a methylene bridge. CMP is commonly used as a ligand in coordination chemistry and as a building block for the synthesis of various organic compounds. It has also been studied for its potential pharmaceutical applications, including as an anti-cancer agent and as a potential treatment for neurodegenerative diseases. CMP is a colorless to pale yellow liquid at room temperature and is insoluble in water, but soluble in organic solvents such as ethanol and acetone.

Check Digit Verification of cas no

The CAS Registry Mumber 70525-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,2 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70525-40:
(7*7)+(6*0)+(5*5)+(4*2)+(3*5)+(2*4)+(1*0)=105
105 % 10 = 5
So 70525-40-5 is a valid CAS Registry Number.

70525-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(cyclohexylidenemethyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-cyclohexylidenemethyl-pyridine

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:70525-40-5 SDS

70525-40-5Downstream Products

70525-40-5Relevant articles and documents

Transition metal-catalyzed intramolecular C-H/olefin coupling

Fujii, Naoaki,Kakiuchi, Fumitoshi,Chatani, Naoto,Murai, Shinji

, p. 939 - 940 (1996)

The ruthenium-and rhodium-catalyzed intramolecular C-H/olefin coupling reactions of 1-(2-pyridyl)-1,5-and 1,6-dienes proceeded regio-and stereoselecively to give 5-or 6-membered ring products.

Aryl-Nickel-Catalyzed Benzylic Dehydrogenation of Electron-Deficient Heteroarenes

Zhang, Pengpeng,Huang, David,Newhouse, Timothy R.

, p. 1757 - 1762 (2020/02/04)

This manuscript describes the first practical benzylic dehydrogenation of electron-deficient heteroarenes, including pyridines, pyrazines, pyrimidines, pyridazines, and triazines. This transformation allows for the efficient benzylic oxidation of heteroarenes to afford heterocyclic styrenes by the action of nickel catalysis paired with an unconventional bromothiophene oxidant.

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