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

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

Used in Organic Synthesis:
2-ETHOXY-4-FORMYL-PHENYL ACETATE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a wide range of chemical reactions, making it a valuable building block for the creation of new molecules with diverse properties and applications.
Used as a Catalytic Agent:
In the field of catalysis, 2-ETHOXY-4-FORMYL-PHENYL ACETATE serves as an effective catalyst for specific chemical reactions. Its ability to lower activation energy and increase reaction rates makes it a useful tool in enhancing the efficiency of various industrial processes.
Used in Petrochemical Additives:
2-ETHOXY-4-FORMYL-PHENYL ACETATE is also employed as an additive in the petrochemical industry. Its incorporation into various formulations can improve the performance characteristics of fuels and lubricants, contributing to enhanced efficiency and reduced environmental impact.

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

• 1026131-44-1 Acetic acid 2-ethoxy-4-thiazolidin-2-yl-phenyl ester 
• 5438-38-0 3-ethoxy 4-hydroxy benzoic acid 
• 1159214-82-0 C₂₈H₂₈N₂O₆ 
• 1124126-22-2 C₁₇H₁₇NO₃ 
• 1138818-47-9 C₁₇H₂₃NO₃ 
• 1215097-92-9 2-ethoxy-4-[(E)-hexadecyliminomethyl]phenyl acetate 
• 1211396-47-2 2-ethoxy-4-[(E)-4-phenoxyphenyliminoethyl]phenyl acetate 

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:

Preparative synthesis of vanillin and vanillal alkanoates

Procedures for preparing vanillin and vanillal alkanoates were developed.

Vanillal esters in reaction with 2-naphthylamine and 1,3-diketones

Analogs of natural alkaloids of acridone series, derivatives of 4-(9-alkyl-11-oxo-7,8,9,10,1,12-hexahydro-benzo[a]acridin-12-yl) and 4-(12-oxo-12H-benzo[f]indeno[1,2-b]quinolin-13-yl)2-ethoxyphenyl carboxylates were synthesized by a three-component conden

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.