142779-20-2 Usage
Chemical structure
1,3-Cyclohexadiene-1-carbonitrile, 2-amino-6-methyl-4,6-bis[2-(2,6,6-trimethyl-1-cyclohexen-1-yl)ethenyl]-, (E,E)is a complex organic molecule with multiple functional groups and a cyclic structure.
Functional groups
The compound contains a nitrile group (C≡N), two amino groups (-NH2), and multiple methyl groups (-CH3).
Cyclic structure
It consists of multiple cyclohexene rings, which are six-membered carbon rings with a double bond.
Classification
The compound is classified as a diene, which means it has two carbon-carbon double bonds in its structure.
Stereochemistry
The compound has an (E,E) configuration, indicating the relative positions of the double bonds in the molecule.
Applications
It is typically used in organic synthesis and chemical research due to its unique structure and properties.
Reactivity
The presence of multiple functional groups in the molecule makes it potentially reactive with various reagents, allowing for the formation of a wide range of products.
Solubility
The compound is likely to be soluble in organic solvents, such as ethanol, acetone, or dichloromethane, due to its nonpolar nature.
Stability
The stability of the compound may depend on factors such as temperature, pH, and the presence of other reactive species.
Synthesis
The compound can be synthesized through various chemical reactions, such as condensation, substitution, or addition reactions, involving appropriate precursors and reagents.
Check Digit Verification of cas no
The CAS Registry Mumber 142779-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,7 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142779-20:
(8*1)+(7*4)+(6*2)+(5*7)+(4*7)+(3*9)+(2*2)+(1*0)=142
142 % 10 = 2
So 142779-20-2 is a valid CAS Registry Number.
142779-20-2Relevant academic research and scientific papers
Valla, Alain,Andriamialisoa, Zo,Labia, Roger
, p. 3359 - 3362 (2000)
New cyclic retinoids from β-ionone and C-14 and C-15 derivatives were synthesised by self-condensation promoted by strong bases. (C) 2000 Published by Elsevier Science Ltd.
An efficient one-pot synthesis of tethered cyclohexadiene enaminonitriles from methyl-ketones: An effective route to quinazolines
Bench, Bennie J.,Suarez, Victor H.,Watanabe, Coran M.H.
, p. 3126 - 3130 (2008/12/22)
The quinazolines represent a useful natural product scaffold with demonstrated activities against disorders such as high blood pressure and benign prostatic hyperplasia. Here we report on the synthesis and biological activity of a series of quinazolines t
The proline and β-lactoglobulin mediated asymmetric self-condensation of β-ionylideneacetaldehyde, retinal and related compounds
Asato,Watanabe,Li,Liu
, p. 3105 - 3108 (2007/10/02)
Proline was found to effectively mediate the asymmetric reaction of β-ionylideneacetaldehyde 1A, retinal and related α,β-unsaturated aldehydes to form their corresponding self-condensation products in reasonable enantiomeric excess (up to 65% ee). This sa
