1483-88-1 Usage
Uses
Used in Organic Synthesis:
2,4-Hexadienamide, N-phenyl-, (E,E)is used as a building block in organic synthesis for its unique reactivity and chemical properties. Its conjugated double bonds allow for various chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Polymer Production:
2,4-Hexadienamide, N-phenyl-, (E,E)is used as a monomer in the production of polymers. Its versatile chemical structure allows for the creation of polymers with specific properties, such as adhesives, coatings, and sealants.
Used in Adhesives Industry:
In the adhesives industry, 2,4-Hexadienamide, N-phenyl-, (E,E)is used as a monomer for the production of high-performance adhesives. Its unique chemical properties contribute to the development of adhesives with enhanced bonding strength and durability.
Used in Coatings Industry:
2,4-Hexadienamide, N-phenyl-, (E,E)is used as a monomer in the coatings industry to produce coatings with improved properties. Its reactivity and chemical properties enable the creation of coatings with enhanced durability, resistance to environmental factors, and aesthetic appeal.
Used in Sealants Industry:
In the sealants industry, 2,4-Hexadienamide, N-phenyl-, (E,E)is used as a monomer to develop high-performance sealants. Its unique chemical structure contributes to the production of sealants with excellent adhesion, flexibility, and resistance to various environmental conditions.
Used in Pharmaceuticals:
2,4-Hexadienamide, N-phenyl-, (E,E)has potential applications in pharmaceuticals due to its versatile chemical structure. It can be used as a building block for the synthesis of pharmaceutical compounds with specific therapeutic properties.
Used in Agrochemicals:
2,4-Hexadienamide, N-phenyl-, (E,E)also has potential applications in agrochemicals. Its unique chemical properties can be utilized in the development of agrochemicals with targeted effects on pests or diseases, contributing to more efficient and sustainable agricultural practices.
However, it is important to note that the handling and use of 2,4-Hexadienamide, N-phenyl-, (E,E)should be done with caution, as it may pose risks to human health and the environment. Proper safety measures and regulations should be followed to minimize any potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 1483-88-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1483-88:
(6*1)+(5*4)+(4*8)+(3*3)+(2*8)+(1*8)=91
91 % 10 = 1
So 1483-88-1 is a valid CAS Registry Number.
1483-88-1Relevant articles and documents
Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives
Narasimhan, Balasubramanian,Judge, Vikramjeet,Narang, Rakesh,Ohlan, Ruchita,Ohlan, Sucheta
, p. 5836 - 5845 (2008/03/18)
A new series of 2,4-hexadienoic acid derivatives (S1-S42) has been synthesized and evaluated as antimicrobial agents against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Candida albicans, and Aspergillus niger. Quantitative structure-activity relationship (QSAR) investigation using Hansch analysis was applied to find out correlation between antimicrobial activities with physicochemical properties of the synthesized compounds. Various physicochemical descriptors and experimentally determined minimum inhibitory concentration values for different microorganisms were used as independent and dependent variables, respectively. The QSAR revealed that topological parameters especially molecular connectivity indices (χ2, 0χv, 2χv) were found to have overall significant correlation with antimicrobial activity of 2,4-hexadienoic acid derivatives. The statistical results of training set, cross-validated r2 and conventional r values gave reliability to the prediction of molecules with activity using QSAR models.
Syntheses and QSAR studies of sorbic, cinnamic and ricinoleic acid derivatives as potential antibacterial agents
Narasimhan,Kothawade,Pharande,Mourya,Dhake
, p. 2828 - 2834 (2007/10/03)
Amides and esters of sorbic, cinnamic and ricinoleic acid have been synthesized and evaluated for their antibacterial activity against gram (+) ve S. aureus, B. subtilis and gram (-) ve E. coli. Most of the compounds have shown moderate to good activity against microorganisms under test. Linear regression analysis of descriptors related to lipophilicity, steric and electronic parameters against antibacterial activity have been performed. QSAR studies indicated the predominance of electronic and steric parameters over the lipophilicity parameters in contributing antibacterial activity.
