58350-97-3

Usage

Chemical class

Dinitriles, known for their diverse range of biological activities.

Usage

Commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

Potential applications

Development of new drugs and pesticides.

Structural features

Thiazole ring fused with a phenyl group.

Structural features

Two nitrile functional groups.

Importance

Understanding its properties and reactivity is crucial for potential use in various applications.

Reactivity

The presence of the thiazole ring, phenyl group, and nitrile groups contributes to the compound's reactivity.

Interaction with biological targets

The structural features of 2-(4-phenyl-2-thiazolyl)propanedinitrile allow for potential interaction with biological targets.

Upstream product

• 5399-30-4 2-oxo-2-phenylethylthiocyanate 
• 109-77-3 malononitrile 

Downstream Products

• 58351-12-5 (3-methyl-4-phenyl-3H-thiazol-2-ylidene)-malononitrile 
• 58351-13-6 methyl-(4-phenyl-thiazol-2-yl)-malononitrile 
• 1264135-59-2 C₁₉H₁₃N₃OS 
• 1264135-81-0 C₂₃H₂₂N₄S 
• 1264136-07-3 (Z)-2-[(5-{[5-(4,5-dimethyl-1,3-dithiol-2-ylidene)methyl]thiophen-2-yl}methylene)-4-phenylthiazol-2-ylidene]malononitrile 
• 1264136-18-6 2-{(Z)-5-[(E)-3-{4-(diethylamino)phenyl}allylidene]-4-phenylthiazol-2-ylidene}malononitrile 
• 1264135-86-5 2-[5-(4,5-dimethyl-1,3-dithiol-2-ylidene)-4-phenylthiazol-2-ylidene]malononitrile 
• 1260019-66-6 N-[(1E,3E,5Z)-5-(2-dicyanomethylene-4-phenylthiazol-2-ylidene)penta-1,3-dienyl]-N-phenylacetamide 
• 1264135-93-4 (Z)-2-{5-[2-(4,5-dimethyl-1,3-dithiol-2-ylidene)ethylidene]-4-phenylthiazol-2-ylidene}malononitrile 
• 1264136-15-3 (Z)-2-[5-(4-diethylaminobenzylidene)-4-phenylthiazol-2-ylidene]malononitrile 
• 1264135-96-7 2-{(Z)-5-[(E)-4-(4,5-dimethyl-1,3-dithiol-2-ylidene)but-2-enylidene]-4-phenylthiazol-2-ylidene}malononitrile 

Relevant academic research and scientific papers

NOVEL PHOTOINITIATORS FOR PHOTOPOLYMERS

The present invention relates to a novel photopolymer formulation comprising a polyol component, a polyisocyanate component, a writing monomer and a photoinitiator comprising a dye of formula (I). The present invention further relates to a holographic medium which contains a photopolymer formulation of the present invention or is obtainable by using same, to the use of a photopolymer formulation of the present invention for producing holographic media and also to a process for producing a holographic medium by using a photopolymer formulation of the present invention.

Azo dye and azo compound

An azo dye including a compound represented by formula (I): wherein R1 represents a hydroxyl group, an aliphatic sulfonyl amino group, an aryl sulfonyl amino group, an aliphatic oxy group, an aryloxy group, or -CH(R2)(R3); R2 and R3 each represent a substituent with a a value of the Hammett's rule in the range of 0.2 or more and less than 1.4, and may be identical to or different from each other; W represents a sulfur atom or -N-(-R4)-; R4 represents a substituent; R5 represents a substituent; X, Y, and Z each represent an atom required for forming a five-membered aromatic heterocycle, where at least one atom of X, Y, and Z represents a nitrogen atom but both X and Y do not represent a carbon atom when Z represents a nitrogen atom; and R6 represents a hydrogen atom or a substituent, n represents 1 or 2, and two R6s may be coupled together to form an aromatic ring or a heteroaromatic ring when n represents 2.