42059-49-4

Basic information

• Product Name: 7-ACETOXY-3-FORMYLCHROMONE
• Synonyms: CHEMBRDG-BB 6567274;7-ACETOXY-3-FORMYLCHROMONE;SPECS AJ-291/34003002;Albb-008110;3-formyl-4-oxo-4H-chromen-7-yl acetate(SALTDATA: FREE);(3-formyl-4-oxo-chromen-7-yl) acetate;(3-formyl-4-oxochromen-7-yl) acetate;(3-methanoyl-4-oxo-chromen-7-yl) ethanoate
• CAS NO: 42059-49-4
• Molecular Formula: C12H8O5
• Molecular Weight: 232.19
• Mol File: 42059-49-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 395.1°C at 760 mmHg
• Flash Point: 178.8°C
• Appearance: /
• Density: 1.457g/cm³
• Vapor Pressure: 1.89E-06mmHg at 25°C
• Refractive Index: 1.644
• CAS DataBase Reference: 7-ACETOXY-3-FORMYLCHROMONE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-ACETOXY-3-FORMYLCHROMONE(42059-49-4)
• EPA Substance Registry System: 7-ACETOXY-3-FORMYLCHROMONE(42059-49-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-43
• Safety Statements: 36/37
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 42059-49-4(Hazardous Substances Data)

Usage

General Description

7-ACETOXY-3-FORMYLCHROMONE, also known as 7-acetoxy-3-formylcoumarin, is a chemical compound that belongs to the class of chromones. It is a derivative of coumarin, a natural chemical found in many plants. 7-ACETOXY-3-FORMYLCHROMONE is known for its potential pharmacological activities, including anti-inflammatory, antioxidant, and anticancer properties. It has been studied for its potential use in the development of new drug therapies. 7-ACETOXY-3-FORMYLCHROMONE is also known for its use in organic synthesis as a starting material for the preparation of various chemical compounds. Its unique structure and potential biological activities make it a subject of interest for further research and development.

InChI:InChI=1/C12H8O5/c1-7(14)17-9-2-3-10-11(4-9)16-6-8(5-13)12(10)15/h2-6H,1H3

Upstream product

• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 42059-48-3 acetic acid 4-acetyl-3-hydroxyphenyl ester 
• 68-12-2 N,N-dimethyl-formamide 
• 75258-58-1 C₉H₁₄ClN₅O₂⁽²⁺⁾*2Cl^(1-) 

Downstream Products

• 1592003-19-4 5-(2,4-dihydroxybenzoyl)-1-hexylpyridin-2(1H)-one 
• 1592003-20-7 t-butyl [2-{5-(2,4-dihydroxybenzoyl)-2-oxopyridin-1(2H)-yl}ethyl]carbamate 
• 1592003-21-8 1-hexyl-5-(2-hydroxy-4-methoxybenzoyl)pyridin-2(1H)-one 
• 1201816-81-0 5-(2-hydroxy-4-methoxybenzoyl)-1-isopropylpyridin-2(1H)-one 
• 1592003-22-9 1-[2-(dimethylamino)ethyl]-5-(2-hydroxy-4-methoxybenzoyl)pyridin-2(1H)-one 
• 1592003-23-0 t-butyl [2-{5-(2-hydroxy-4-methoxybenzoyl)-2-oxopyridin-1(2H)-yl}ethyl]carbamate 
• 1592003-24-1 5-(2-hydroxy-4-methoxybenzoyl)-1-(2-hydroxyethyl)pyridin-2(1H)-one 
• 1201816-77-4 1-cyclohexyl-5-(2-hydroxy-4-methoxybenzoyl)pyridin-2(1H)-one 
• 1201816-79-6 1-butyl-5-(2-hydroxy-4-methoxybenzoyl)pyridin-2(1H)-one 
• 1388221-20-2 1-butyl-5-(2,4-dihydroxybenzoyl)pyridin-2(1H)-one 
• 42059-55-2 7-hydroxy-3-formylchromone 
• 124980-74-1 β-(7-Acetoxy-3-chromonyl)acrolein 

Relevant articles and documents

Synthesis, 1H and 13C NMR assignment of novel 2-pyridone derivatives

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Alzheimer's disease is the most common cause of dementia in the elderly, and no disease-modifying therapy is yet available for this devastating pathology. Deposition of different physicochemical forms of amyloid-β peptides is a critical phase in the patho

Derivatives of 1,3,5-Triazine: Part III - Cyanuric Chloride-Dimethylformamide as a New Reagent for Synthesis of Amides, Esters, Aldehydes and for Dehydration Reactions

Cyanuric chloride reacts with dimethylformamide to form a complex (I), which can be used directly for the synthesis of amides, esters, relatively simple peptides, aldehydes and for dehydration reactions.