57009-53-7

Basic information

• Product Name: Benzoic acid, 3-acetyl-4-hydroxy-, ethyl ester
• CAS NO: 57009-53-7
• Molecular Formula: C11H12O4
• Molecular Weight: 208.214
• Mol File: 57009-53-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-acetyl-4-hydroxy-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-acetyl-4-hydroxy-, ethyl ester(57009-53-7)
• EPA Substance Registry System: Benzoic acid, 3-acetyl-4-hydroxy-, ethyl ester(57009-53-7)

Safety Data

• Hazardous Substances Data: 57009-53-7(Hazardous Substances Data)

Upstream product

• 2345-34-8 4-acetyloxy-benzoic acid 
• 13031-45-3 ethyl 4-acetoxybenzoate 
• 4869-46-9 1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde 
• 123-54-6 acetylacetone 
• 141-52-6 sodium ethanolate 
• 74442-98-1 5-(2,2-Diacetylvinyl)-1,3-dimethyluracil 
• 16357-40-7 3-acetyl-4-hydroxybenzoic acid 

Downstream Products

• 1242248-34-5 (E)-ethyl 4-hydroxy-3-(3-(4-(4-phenoxybutoxy)phenyl)acryloyl)benzoate 
• 105639-12-1 5-{5-[4-(4,5-Dihydro-2-oxazolyl)-2-acetylphenoxy]pentyl}-3-methylisoxazole 
• 105639-25-6 2-acetyl-4-(4,5-dihydro-2-oxazolyl)phenol 
• 102298-02-2 ethyl 3-acetyl-5-cyano-4-hydroxybenzoate 
• 90844-13-6 4-hydroxyisophthalic acid 1-ethyl ester 
• 65372-54-5 2,2-dimethyl-4-chromanone-6-carboxylic acid 
• 1026852-20-9 4-Hydroxy-3-(3-oxo-3-quinolin-2-yl-propionyl)-benzoic acid ethyl ester 
• 102298-00-0 ethyl 3-acetyl-5-bromo-4-hydroxybenzoate 

Relevant articles and documents

Synthesis and insecticidal activity of chromanone and chromone analogues of diacylhydrazines

Diacylhydrazine derivatives have been identified as one of the most important insect growth regulators. A variety of diacylhydrazine derivatives were designed and synthesized in recent years due to their unique action mechanism, simple structure, and environmental benign character. This paper describes the molecular design, synthesis, and insecticidal activities of a series of chromanone and chromone analogues of diacylhydrazine derivatives. The preliminary bioassay showed that some of the chromanone analogues exhibited good insecticidal activity against Mythima separata at the dosage of 500 mg L-1. The present work demonstrated that replacement of the chroman ring of ANS-118, a commercial insecticide, with chromanone moiety could result in new compounds with high potent insecticidal activity.

A Novel Ring Transformation of Uracil into the Benzene Ring System

Reaction of 5-formyl-1,3-dimethyluracil with some active methylene compounds in the presence of base causes novel ring transformations to give the p-hydroxybenzoates and the nicotinate.