1520-20-3

Usage

Uses

Used in Pharmaceutical Industry:
P-Vinylphenyl isothiocyanate is used as a reactive intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drug candidates with potential therapeutic applications.
Used in Agricultural Chemical Industry:
In the agricultural sector, P-Vinylphenyl isothiocyanate serves as a key intermediate in the production of agricultural chemicals. Its reactivity enables the creation of novel compounds designed to address specific needs in crop protection and enhancement.
Used in Specialty Chemicals Production:
P-Vinylphenyl isothiocyanate is utilized in the synthesis of specialty chemicals, which are tailored for specific industrial applications. Its versatility as a reactive intermediate contributes to the development of innovative products with unique properties.
Used in Antimicrobial Applications:
P-Vinylphenyl isothiocyanate has been studied for its antimicrobial properties, making it a potential candidate for use in applications requiring the inhibition of microbial growth, such as in medical or industrial settings.
Used in Anticancer Research:
P-VINYLPHENYL ISOTHIOCYANATE has shown promise in anticancer research, warranting further investigation into its potential as a therapeutic agent against various types of cancer. Its biological activity may be harnessed to develop new treatments or enhance existing ones.

InChI:InChI=1/C9H7NS/c1-2-8-3-5-9(6-4-8)10-7-11/h2-6H,1H2

Upstream product

• 463-71-8 thiophosgene 
• 1520-21-4 4-vinyl benzylamine 

Downstream Products

• 1483-59-6 N-<4-Vinyl-phenyl>-thioharnstoff 

Relevant academic research and scientific papers

Determining the regioregularity in alkyne polycarbodiimides and their orthogonal modification of side chains to yield perfectly alternating functional polymers

To understand the structure-property relationship in functional macromolecules through side chain modulation, both the accurate determination of the position of modifiable groups along the polymer chain and their subsequent modifications using high fideli

Determining the regioregularity in alkyne polycarbodiimides and their orthogonal modification of side chains to yield perfectly alternating functional polymers

To understand the structure-property relationship in functional macromolecules through side chain modulation, both the accurate determination of the position of modifiable groups along the polymer chain and their subsequent modifications using high fidelity methods are crucial. In this report, the polymer microstructure of a helical alkyne polycarbodiimide has directly been probed through 15N NMR spectroscopy on isotopic labeled poly(N-(3-ethynylphenyl)-15N′-hexyl)carbodiimide and found to be a highly regioregular polymer structure. This polymer undergoes facile and quantitative CuAAC "click" chemistry, yielding perfectly alternating functional polymers. Advances have been made through the synthesis of new optically active alkyne polycarbodiimides with two independently modifiable pendant groups per repeat unit of polymers. Orthogonal postmodifications of the pendant groups were then performed to incorporate two different sets of small molecules in the repeat unit of polymers in a controlled manner and under mild reaction conditions using either sequential CuAAC "click" reactions when two dissimilar alkyne groups are present or a combination of CuAAC and thiol-ene click chemistries when pendant groups bear alkyne and vinyl moieties.