143769-53-3

Basic information

• Product Name: Benzoic acid, 2-acetyl-4-methyl-, ethyl ester
• CAS NO: 143769-53-3
• Molecular Formula: C12H14O3
• Molecular Weight: 206.241
• Mol File: 143769-53-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-acetyl-4-methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-acetyl-4-methyl-, ethyl ester(143769-53-3)
• EPA Substance Registry System: Benzoic acid, 2-acetyl-4-methyl-, ethyl ester(143769-53-3)

Safety Data

• Hazardous Substances Data: 143769-53-3(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 143769-40-8 7-acetyl-2-methoxy-5-methyltropone 
• 124-46-9 guanidine hydrogen carbonate 
• 22661-87-6 1-methylguanidine hydrochloride 
• 143769-37-3 3-acetyl-2-methoxy-5-methyltropone 
• 182567-82-4 2-hydroxy-5-methylcetophenone ethoxycarbonylhydrazone 
• 78-79-5 isoprene 

Relevant articles and documents

β-Chloro-α,β-unsaturated carbonyls as convenient precursors of highly substituted benzenes

The Diels–Alder reactions of three β-chloro-α,β-unsaturated carbonyl compounds 1–3 with different dienes were carried out to afford highly functionalized cyclohexenes 4–9, bearing quaternary centers, in good yields. These cycloadducts (CAs) undergo dehydr

Reactions of 3-Isopropyl-, 3-Isopropenyl-, and 3-Acetyltropolone Methyl Ethers with Guanidines. Synthesis of 9H-Cycloheptapyrimidin-9-ones and Cycloheptimidazoles

3-Isopropyl- and 3-isopropenyltropolone methyl ethers reacted with guanidine, 1-methylguanidine, and 1,1-dimethylguanidine to afford the corresponding 4-isopropyl- and 4-isopropenylcycloheptimidazoles 4a-f, respectively.The reactions of 3-acetyl-2-methoxytropones 2c-e with guanidines afforded 4-methyl-9H-cycloheptapyrimidin-9-ones 8a-i, while the reactions of 7-acetyl-2-methoxytropones 3c,d produced 4-acetylcycloheptimidazoles 4g-l.From these reactions, several minor products were also isolated.