65996-11-4 Usage
Pentadienoic acid group
A group consisting of two carbon-carbon double bonds separated by a single bond in a five-carbon chain, contributing to the compound's reactivity and potential applications in organic synthesis.
Cyano group
A cyanide group (CN) bonded to a carbon atom, providing the compound with a strong electron-withdrawing effect and contributing to its potential use as a photoinitiator.
Dimethylamino group
A nitrogen atom bonded to two methyl groups (CH3), providing the compound with basicity and potential for hydrogen bonding, which can affect its solubility and reactivity.
Ethyl ester functional group
An ester group (C=O) bonded to an ethyl group (CH2CH3), providing the compound with potential for hydrolysis and reactivity in organic synthesis.
Reagent in organic synthesis
The compound's reactive functional groups make it a useful reagent in organic synthesis, allowing for the formation of a variety of new compounds through chemical reactions.
Building block in pharmaceuticals and agrochemicals
The compound's unique structure and reactivity make it a valuable building block in the production of various pharmaceuticals and agrochemicals, with potential for the development of new drugs and pesticides.
Potential as a photoinitiator
The presence of the cyano group gives the compound potential as a photoinitiator for polymerization reactions, allowing for the formation of polymers with specific properties.
Precursor for bioactive molecules
The compound's unique structure and functional groups make it a potential precursor for the synthesis of bioactive molecules, which could have applications in medicine or agriculture.
Toxic if ingested or inhaled
The compound can be toxic if ingested or inhaled, and should be handled with caution to avoid exposure.
Skin and eye irritation
The compound may cause skin and eye irritation upon contact, and appropriate personal protective equipment should be worn when handling it.
Flammable
The compound has the potential to be flammable, and should be stored and handled in accordance with proper safety protocols to avoid fire or explosion hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 65996-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,9 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65996-11:
(7*6)+(6*5)+(5*9)+(4*9)+(3*6)+(2*1)+(1*1)=174
174 % 10 = 4
So 65996-11-4 is a valid CAS Registry Number.
65996-11-4Relevant articles and documents
PIPERIDINE COMPOUNDS AS PCSK9 INHIBITORS
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, (2018/11/21)
One aspect of the invention relates to a series of new PCSK9 inhibitor compounds comprising piperidine ring structures, including compounds of formula (I) and/or pharmaceutically acceptable salts thereof. Another aspect of the invention relates to methods of treating PCSK9 receptor related diseases comprising administration of one or more compounds of formula (I) or a pharmaceutically acceptable salt thereof.
HETEROCYCLIC COMPOUNDS AND USES THEREOF
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, (2013/03/26)
Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.
SYNTHESIS OF 3-AMINO-2-CHLORO-4-METHYLPYRIDINE FROM ACETONE AND ETHYL CYANOACETATE
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Page/Page column 5, (2010/02/14)
A method for making 3-amino-2-chloro-4-methylpyridine from acetone and ethyl cyanoacetate, as depicted in the following reaction scheme.
