3179-01-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C), 11 hydrogen (H), 3 nitrogen (N), and 4 oxygen (O) atoms.
Explanation
Nitro compounds are organic compounds that contain one or more nitro groups attached to a carbon atom. The presence of nitro groups can affect the compound's reactivity and stability.
Explanation
The benzene ring is a six-carbon atom ring with alternating single and double bonds, which provides the molecule with its aromatic properties.
Explanation
The (E) and (Z) configurations describe the relative positions of the substituents around the double bond in the nitroethylene side chains. (E) indicates that the substituents are on opposite sides of the double bond, while (Z) indicates that they are on the same side.
Explanation
The compound serves as a starting material or intermediate in the synthesis of more complex organic molecules, which can be used in various applications.
Explanation
Due to its unique structure and properties, 1-[(E)-2-nitroethenyl]-4-[(Z)-2-nitroethenyl]benzene has potential applications in the development of new materials and pharmaceuticals.
Explanation
The compound's reactivity in chemical reactions can be affected by the presence of nitro groups and the stereochemistry of the nitroethylene side chains, which can determine the compound's behavior and the types of reactions it can undergo.
Explanation
The compound's unique properties and potential applications make it a versatile chemical that can be utilized in various scientific and industrial fields, such as the development of new materials, pharmaceuticals, and other organic compounds.
Nitro compound
Contains nitro groups (-NO2)
Benzene ring
Aromatic ring structure
Nitroethylene side chains
Two side chains attached to the benzene ring
Stereochemistry
(E) and (Z) configurations
Building block
Used in the synthesis of organic molecules
Applications
Materials science and pharmaceutical research
Reactivity
Influenced by stereochemistry and nitro groups
Versatility
Important in scientific and industrial fields
Check Digit Verification of cas no
The CAS Registry Mumber 3179-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3179-01:
(6*3)+(5*1)+(4*7)+(3*9)+(2*0)+(1*1)=79
79 % 10 = 9
So 3179-01-9 is a valid CAS Registry Number.
3179-01-9Relevant academic research and scientific papers
Regiospecific synthesis of novel cyclic nitrostyrenes and 3-substituted 2-nitronaphthalenes
Keene, Craig,Kuerti, Laszlo
supporting information, p. 1719 - 1729 (2013/07/26)
A two-step, practical, regiospecific, and readily scalable benzannulation protocol for the preparation of novel 3-alkyl- and 3-aryl-substituted 2-nitronaphthalenes is disclosed. Addition of a β-nitrostyrene or nitroalkene to a solution of freshly prepared lithiated o-tolualdehyde tert-butyl imine first leads to the formation of a nitronate, via rapid 1,4-addition, then an intramolecular aza-Henry reaction takes place to afford a six-membered carbocycle. Subsequent treatment of the reaction mixture with aqueous acid affords novel substituted cyclic nitrostyrenes that can be conveniently aromatized via a one-pot radical-induced bromination and elimination sequence to furnish the corresponding 3-alkyl- or 3-aryl-2-nitronaphthalenes in excellent yields. The straightforward syntheses of 2-aminonaphthalenes, substituted BINAMs, 2-naphthols as well as tricyclic fused 1,2,3-triazoles are also described. Georg Thieme Verlag Stuttgart. New York.
