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Cyclohexanone, 2-[(dimethylamino)methylene]-, also known as 2-(dimethylamino)methylenecyclohexanone or DMCM, is an organic compound with the chemical formula C9H15NO. It is a colorless to pale yellow liquid with a strong, pungent odor. Cyclohexanone, 2-[(dimethylamino)methylene]- is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other chemicals. DMCM is known for its reactivity and can undergo various chemical transformations, making it a valuable building block in organic synthesis. It is also used as a solvent and a reagent in various chemical reactions. Due to its potential health and environmental risks, proper handling and disposal procedures are essential when working with this chemical.

6135-19-9

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6135-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6135-19-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6135-19:
(6*6)+(5*1)+(4*3)+(3*5)+(2*1)+(1*9)=79
79 % 10 = 9
So 6135-19-9 is a valid CAS Registry Number.

6135-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((dimethylamino)methylene)cyclohexanone

1.2 Other means of identification

Product number -
Other names 2-(dimethylaminomethylene)cyclohexanone

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:6135-19-9 SDS

6135-19-9Relevant academic research and scientific papers

Discovery of CDK5 Inhibitors through Structure-Guided Approach

Khair, Nishat Z.,Lenjisa, Jimma L.,Tadesse, Solomon,Kumarasiri, Malika,Basnet, Sunita K. C.,Mekonnen, Laychiluh B.,Li, Manjun,Diab, Sarah,Sykes, Matthew J.,Albrecht, Hugo,Milne, Robert,Wang, Shudong

supporting information, p. 786 - 791 (2019/05/17)

Specific abrogation of cyclin-dependent kinase 5 (CDK5) activity has been validated as a viable approach for the development of anticancer agents. However, no selective CDK5 inhibitor has been reported to date. Herein, a structure-based in silico screenin

BIARYL PYRAZOLES AS NRF2 REGULATORS

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Page/Page column 285; 286, (2017/08/01)

The present invention relates to biaryl pyrazole compounds, methods of making them, pharmaceutical compositions containing them and their use as NRF2 regulators.

Discovery, synthesis, and structure-activity relationships of 2-aminoquinazoline derivatives as a novel class of metabotropic glutamate receptor 5 negative allosteric modulators

Kubas, Holger,Meyer, Udo,Krueger, Bjoern,Hechenberger, Mirko,Vanejevs, Maksims,Zemribo, Ronalds,Kauss, Valerjans,Ambartsumova, Raisa,Pyatkin, Ilya,Polosukhin, Alexey I.,Abel, Ulrich

supporting information, p. 4493 - 4500 (2013/08/23)

A virtual screening approach using various in silico methodologies led to the discovery of 2-(m-tolylamino)-7,8-dihydroquinazolin-5(6H)-one (1) as a moderately active negative allosteric modulator (NAM) of the metabotropic glutamate receptor subtype 5 (mGluR5) showing high selectivity against the subtype mGluR1. Modifications of the parent compound by rational design yielded a series of highly potent derivatives which will serve as valuable starting points for further hit-to-lead optimization efforts toward a suitable drug candidate for the treatment of l-DOPA induced dyskinesia.

METABOTROPIC GLUTAMATE RECEPTOR MODULATORS

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Page/Page column 50-51, (2012/07/13)

The invention relates to heterocyclic derivatives as well as their pharmaceutically acceptable salts. The invention further relates to a process for the preparation of such compounds. The compounds of the invention are mGluR5 modulators and are therefore useful for the control and prevention of acute and/or chronic neurological disorder

Synthesis of δ-tributylstannyl-α,βγ, δ-unsaturated aldehydes from pyridines

Michels, Theo D.,Rhee, Jong Uk,Vanderwal, Christopher D.

body text, p. 4787 - 4790 (2009/05/07)

(Equation Presented) Zincke aldehydes, which are readily available from the ring-opening reaction of pyridinium salts, are easily converted into δ-tributylstannyl-α,β,γ,δ-unsaturated aldehydes (stannyldienals) by the action of tributylstannyllithium. This reaction appears to proceed via 1,6-stannyllithium addition/elimination of lithium dialkylamide. Several stannyldienals of significant utility for the synthesis of polyene natural products have been made by this route, which proceeds in modest yields, but is successful on multigram scale using inexpensive reagents. Simple stannylenals and stannylenones are similarly available from the corresponding vinylogous amides.

Tricyclic 6-alkylidene-penems as class-D beta-lactamases inhibitors

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Page/Page column 26, (2010/11/25)

This invention relates to certain tricyclic 6-alkylidene penems which act as a inhibitor of class-D enzymes. β-Lactamases hydrolyze β-lactam antibiotics, and as such serve as the primary cause of bacterial resistance. The compounds of the present inventio

THE SYNTHESIS OF MANNICH BASES FROM KETONES AND ESTERS VIA ENAMINONES.

Schuda, Francis Paul,Ebner, Cynthia B.,Morgan, Tina M.

, p. 2567 - 2570 (2007/10/02)

The reactions of a series of activated methylene compounds with amide acetals to form high yields of enaminones is described.Further conversion to the Mannich bases via reduction with lithium aluminium hydride is also covered.

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