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N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline CAS:70627-52-0

Short Description:

Catalog Number: XD96282
Cas: 70627-52-0
Molecular Formula: C20H16FNO
Molecular Weight: 305.35
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Product Detail

Product Tags

Catalog Number XD96282
Product Name N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline
CAS 70627-52-0
Molecular Formula C20H16FNO
Molecular Weight 305.35
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline is a chemical compound that belongs to the class of benzylidene-based compounds. This compound contains a benzylidene group attached to a 4-fluoroaniline moiety, which gives it unique properties and potential effects.One of the potential effects of N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline is its potential as an organic dye or pigment. Compounds with benzylidene groups often exhibit interesting color properties due to their extended π-conjugation system. The presence of the 4-fluoroaniline moiety in this compound can further enhance its color properties. This makes N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline a candidate for applications in dyeing, pigmentation, or as a colorimetric agent.Furthermore, the presence of the benzylidene group in this compound suggests that it could have potential as a photosensitive material. Benzylidene compounds are known for their photochromic behavior, meaning they can undergo reversible color changes upon exposure to light. This property has been utilized in applications such as photochromic lenses, optical data storage, and security inks.Another potential effect of N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline is its potential as a pharmaceutical intermediate. Substituted anilines have been widely used as building blocks in the synthesis of a variety of drugs. The presence of both benzylidene and fluoro groups in this compound can offer further opportunities for structural modification and optimization to develop new pharmaceutical agents.Additionally, this compound may have potential biological activities on its own. Fluorine substitution at the 4-position of an aromatic ring can alter the electronic and steric properties of the compound, potentially influencing its interactions with biological targets. Further research would be required to evaluate any specific biological effects of N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline on different biological systems.In conclusion, N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline is a compound with potential effects in various fields. Its color properties, photochromic behavior, and potential as a pharmaceutical intermediate make it an interesting compound for further exploration and study. Its specific effects and applications would depend on the specific field of interest and the structural modifications made to the compound.


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    N-(4-(Benzyloxy)benzylidene)-4-fluoroaniline CAS:70627-52-0