1483-88-1

Basic information

• Product Name: 2,4-Hexadienamide, N-phenyl-, (E,E)-
• CAS NO: 1483-88-1
• Molecular Formula: C12H13NO
• Molecular Weight: 187.241
• Mol File: 1483-88-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4-Hexadienamide, N-phenyl-, (E,E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Hexadienamide, N-phenyl-, (E,E)-(1483-88-1)
• EPA Substance Registry System: 2,4-Hexadienamide, N-phenyl-, (E,E)-(1483-88-1)

Safety Data

• Hazardous Substances Data: 1483-88-1(Hazardous Substances Data)

Usage

General Description

2,4-Hexadienamide, N-phenyl-, (E,E)-, also known as soramid, is a chemical compound that belongs to the class of amides. It is commonly used as a building block in organic synthesis and as a monomer in the production of polymers. 2,4-Hexadienamide, N-phenyl-, (E,E)- is characterized by its two conjugated double bonds in the E,E configuration, which gives it unique reactivity and chemical properties. It is often used in the manufacturing of various products such as adhesives, coatings, and sealants. Additionally, it has potential applications in pharmaceuticals and agrochemicals due to its versatile chemical structure. However, its handling and use should be done with caution, as it may pose risks to human health and the environment.

Upstream product

• 62-53-3 aniline 
• 2614-88-2 sorbinyl chloride 
• 110-44-1 sorbic Acid 
• 143372-04-7 Hex-2-ynoic acid phenylamide 
• 504-60-9 penta-1,3-diene 
• 103-71-9 phenyl isocyanate 
• 14506-08-2 hexa-2t,4t-dienoyl-carbonic acid ethyl ester 

Downstream Products

• 1332483-23-4 N-phenyl-13-apo-β-caroten-13-amide 
• 1332483-28-9 N-phenyl-14'-apo-β-caroten-14'-amide 
• 2889-65-8 1-<2-Methyl-cyclopropyl>-cyclopropan-carbonsaeure-(2)-anilid 

Relevant articles and documents

Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives

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.

Internal Redox Catalyzed by Triphenylphosphine

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