72207-94-4

Basic information

• Product Name: 2-ETHOXY-4-FORMYL-PHENYL ACETATE
• Synonyms: AKOS B004453;2-ETHOXY-4-FORMYL-PHENYL ACETATE;ETHYL VANILLIN ACETATE;4-(acetyloxy)-3-ethoxy-benzaldehyd;4-acetoxy-3-ethoxybenzaldehyde;Benzaldehyde, 4-(acetyloxy)-3-ethoxy-;4-(Acetyloxy)-3-ethoxybenzaldehyde
• CAS NO: 72207-94-4
• Molecular Formula: C₁₁H₁₂O₄
• Molecular Weight: 208.21
• Product Categories: Inhibitors
• Mol File: 72207-94-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 45 °C
• Boiling Point: 267.4°C (rough estimate)
• Flash Point: 131.9 °C
• Appearance: /
• Density: 1.0627 (rough estimate)
• Vapor Pressure: 0.000904mmHg at 25°C
• Refractive Index: 1.4389 (estimate)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Solubility: soluble in Methanol
• Water Solubility: Soluble in water (986.4 mg / L) at 25°C.
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2-ETHOXY-4-FORMYL-PHENYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ETHOXY-4-FORMYL-PHENYL ACETATE(72207-94-4)
• EPA Substance Registry System: 2-ETHOXY-4-FORMYL-PHENYL ACETATE(72207-94-4)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• RTECS: CU4381000
• TSCA: Yes
• HazardClass: IRRITANT
• Hazardous Substances Data: 72207-94-4(Hazardous Substances Data)

Usage

Uses

4-Acetoxy-3-ethoxybenzaldehyde is used in organic synthesis. It is used as catalytic agent; petrochemical additive.

InChI:InChI=1/C11H12O4/c1-3-14-11-6-9(7-12)4-5-10(11)15-8(2)13/h4-7H,3H2,1-2H3

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 121-33-5 vanillin 

Downstream Products

• 1211396-47-2 2-ethoxy-4-[(E)-4-phenoxyphenyliminoethyl]phenyl acetate 
• 1236308-63-6 methyl (E,S)-2-(4-acetyloxy-3-ethoxybenzylideneamino)-3-methylbutyrate 
• 1427307-72-9 4-(1,3-dioxan-2-yl)-2-ethoxyphenyl acetate 
• 1417183-50-6 C₁₉H₂₁NO₄*ClH 
• 1417182-61-6 C₁₉H₂₁NO₄ 
• 1314034-97-3 2-(4-acetoxy-3-ethoxyphenyl)-5-methyl-1H-benzimidazole 
• 1198407-39-4 C₂₃H₂₃NO₃ 
• 1198406-63-1 C₂₃H₂₁NO₃ 

Relevant articles and documents

1 -HYDROXY-BENZOOXABOROLES AS ANTIPARASITIC AGENTS

Provided are compounds useful for controlling endoparasites both in animals and agriculture. Further provided are methods for controlling endoparasite infestations of an animal by administering an effective amount of a compound as described above, or a pharmaceutically acceptable salt thereof, to an animal, as well as formulations for controlling endoparasite infestations using the compounds described above or an acceptable salt thereof, and an acceptable carrier. The claimed compounds are described by the following Markush formula:A typical example for a compound according to above formula is: A typical example for a compound according to above formula is:

Reactions of vanillin and vanillal esters with 6-quinolylamine and phenidone

Previously unknown 2-methoxy(or ethoxy)-4-(11-oxo-9-phenyl-7,8,9,10,11,12- hexahydrobenzo[b][4,7]phenanthrolin-12-yl)phenyl esters of carboxylic acids were prepared by ternary condensation of vanillin or vanillal alkanoates with 6-quinolylamine and Phenid

Synthesis and evaluation of novel thiazolidine derivatives as thromboxane A2 receptor antagonists

A series of 3-benzoyl or 3-phenylsulfonyl-2-substituted thiazolidine derivatives were synthesized, and evaluated for their thromboxane A2 (TXA2) receptor-antagonizing effect on (15S)-15-hydroxy-11α,9α- (epoxymethano)prosta-5(Z),13(E)-dienoic acid (U-46619)-induced aggregation of rabbit platelet-rich plasma (PRP). A simple 2-arylthiazolidine derivative, 3- benzoyl-2-(4-hydroxy-3-methoxyphenyl)thiazolidine (5a), showed mild TXA2 receptor antagonist activity. Modification of 5a led to 2-chloro-4-[3-(4- chlorophenylsulfonyl)thiazolidin-2-ylmethyl]phenoxyaretic acid (29d), which showed 10 times more potent TXA2 receptor antagonist activity than 5a.