2597-54-8

Basic information

• Product Name: ACETYLURETHANE
• Synonyms: acetyl-carbamicaciethylester;ethyln-acetylcarbamate;n-acetylethylcarbamate;ACETYLURETHANE;ETHYL ACETYLCARBAMATE;Carbamic acid, acetyl-, ethyl ester;Acetylcarbamic acid ethyl ester;N-Acetylcarbamic acid ethyl ester
• CAS NO: 2597-54-8
• Molecular Formula: C₅H₉NO₃
• Molecular Weight: 131.13
• Mol File: 2597-54-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 261.22°C (rough estimate)
• Flash Point: °C
• Appearance: /
• Density: 1.3075 (rough estimate)
• Refractive Index: 1.4860 (estimate)
• CAS DataBase Reference: ACETYLURETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: ACETYLURETHANE(2597-54-8)
• EPA Substance Registry System: ACETYLURETHANE(2597-54-8)

Safety Data

• Hazardous Substances Data: 2597-54-8(Hazardous Substances Data)

Usage

Description

Acetylurethane, also known as ethyl acetylurethane, is a chemical compound that is a derivative of urethane. It is classified as an organic compound and is known for its good solvent resistance and fast-drying properties. Acetylurethane is commonly used in industrial applications due to its versatility and ability to improve the properties of various materials.

Uses

Used in Adhesives Production:
Acetylurethane is used as a component in the production of adhesives for its ability to improve the solvent resistance and fast-drying properties of the adhesive.
Used in Coatings Production:
Acetylurethane is used as a component in the production of coatings, where it serves as a crosslinker to enhance the durability and performance of the coating.
Used in Inks Production:
Acetylurethane is used in the production of inks to improve their solvent resistance and fast-drying properties, resulting in better print quality and performance.
Used in Polyurethane Coatings Production:
Acetylurethane is used as a crosslinker in the production of polyurethane coatings, which enhances the overall performance and durability of the coatings.
Used in Pharmaceutical Synthesis:
Acetylurethane is used in the synthesis of pharmaceuticals, where it can contribute to the development of new drugs and improve the properties of existing ones.
Used in Pesticide Synthesis:
Acetylurethane is also used in the synthesis of pesticides, where it can help create more effective and durable products for agricultural and other applications.

InChI:InChI=1/C5H9NO3/c1-3-9-5(8)6-4(2)7/h3H2,1-2H3,(H,6,7,8)

Upstream product

• 506-96-7 Acetyl bromide 
• 51-79-6 urethane 
• 89736-51-6 ethyl N-chloro-N-acetylcarbamate 
• 110-83-8 cyclohexene 
• 3998-25-2 acetyl isocyanate 
• 64-17-5 ethanol 

Downstream Products

• 618-42-8 1-piperidin-1-yl-ethanone 
• 2158-03-4 1-piperidinecarboxamide 
• 591-07-1 acetylurea 
• 591-62-8 N-(ethoxycarbonyl)butylamine 
• 32772-88-6 N-acetyl-N'-(2-methoxy-phenyl)-urea 
• 102-03-4 1-acetyl-3-phenylurea 
• 103-84-4 Acetanilid 
• 22863-25-8 5-methyl-2-(4-nitro-phenyl)-1,2-dihydro-[1,2,4]triazol-3-one 
• 857829-17-5 [1-(4-phenyl-thiosemicarbazono)-ethyl]-carbamic acid ethyl ester 
• 933-19-7 6-methyl-1,3,5-triazine-2,4(1H,3H)-dione 
• 617-07-2 N,N'-bis(2-methylphenyl)urea 
• 117514-22-4 N-acetyl-N'-m-tolyl-urea 
• 591-38-8 acetylbiuret 
• 7664-41-7 ammonia 

Relevant articles and documents

The photochemical addition of N-haloamides to olefins: a comparison of cyclic and acyclic N-halo-N-alkylamides and N-halo-N-acylamides (N-haloimides)

Upon photochemical decomposition in the presence of cyclohexene and 1-octene, an N-halo-N-acylamide (N-haloimide) leads to better yields of addition than its N-halo-N-alkyl analogue, and cyclic N-halo-N-alkyl and N-halo-N-acylamides add more efficiently than their acyclic analogues.The yields of addition were higher with N-chlorosuccinimide which has been added also to 1-methylcyclohexene than with N-bromosuccinimide which did not add to 1-methylcyclohexene.