5840-81-3

Usage

Uses

Used in Photoimaging Industry:
2-THIOXOTETRAHYDRO-1,3-OXAZOLE is used as a photoimaging material for its ability to interact with light, which makes it a valuable component in the development of advanced imaging technologies. Its chemical properties allow it to be integrated into the manufacturing process of photoresists, photographic films, and other imaging devices that require sensitivity to light for their operation.
The specific application reason for using 2-THIOXOTETRAHYDRO-1,3-OXAZOLE in the photoimaging industry is its light-sensitive nature, which enables it to play a crucial role in the formation of images when exposed to light. This property is particularly useful in the development of high-resolution imaging systems and materials that require precise control over the exposure process.

InChI:InChI=1/C3H5NOS/c6-3-4-1-2-5-3/h1-2H2,(H,4,6)

Upstream product

• 71-23-8 propan-1-ol 
• 59565-09-2 2-(vinyloxy)ethyl isothiocyanate 
• 65-85-0 benzoic acid 
• 100-51-6 benzyl alcohol 
• 71-36-3 butan-1-ol 
• 108-93-0 cyclohexanol 
• 67-56-1 methanol 

Downstream Products

• 105550-85-4 ((1S,2R)-2-Hydroxymethyl-cyclohexyl)-methyl-dithiocarbamic acid; compound with triethyl-amine 
• 120627-65-8 2-benzylthio-Δ²-1,3-oxazoline 
• 75527-98-9 2-Thioxo-oxazolidine-3-carboximidic acid p-tolyl ester 
• 137578-87-1 N-isobutyryloxazolidine-2-thione 
• 137578-86-0 2-phenyl-1-(2-thioxooxazolidin-3-yl)ethan-1-one 
• 14125-75-8 2,3,4,6-tetra-O-benzoyl-D-hydroxyglucal 
• 868532-38-1 acetic acid 3-phenyl-1-(2-thioxo-oxazolidine-3-carbonyl)-propyl ester 
• 868532-36-9 acetic acid 1-benzyl-2-oxo-2-(2-thioxo-oxazolidin-3-yl)-ethyl ester 
• 868532-34-7 acetic acid 2-oxo-1-phenyl-2-(2-thioxo-oxazolidin-3-yl)-ethyl ester 
• 85430-60-0 3-nitro-1,3-oxazolidine-2-one 

Relevant academic research and scientific papers

VINYL ETHERS CONTAINING AN ISOTHIOCYANATE GROUP VII. REACTION WITH CARBOXYLIC ACIDS

The reaction of 2-vinyloxyethyl isothiocyanate with aliphatic (saturated, unsaturated) and aromatic carboxylic acids leads quantitatively to partial acylals with isocyanate groups.The process takes place at room temperature or with moderate heating and, as a rule, without solvents in the presence of catalytic amounts of heptafluorobutyric acids.From the products of the reaction with benzoic and saturated aliphatic acids 1,3-oxazolidine-2-thione and its polymer were isolated in small amounts (5-7percent) in addition to the respective acylals.

VINYL ETHERS CONTAINING AN ISOTHIOCYANATE GROUP II, SYNTHESIS OF THE ACETALS OF ISOTHIOCYANATOETHANOL

The reaction of the simplest alcohols with 2-vinyloxyethyl isothiocyanate under electrophilic conditions leads to previously unknown acetals containing an isothiocyanate group.Under the reaction conditions (0.2-1.3 wtpercent of perfluorobutyric acid, 40-80, 0.6-3 h) 1,3-oxazolidine-2-thione is formed in addition to the corresponding acetals.The conditions were found which make it possible to direct the reaction toward the preferential formation of either 1,3-oxazolidine-2-thione or the 2-isothiocyanatoethyl acetals of acetaldehyde.