284044-35-5

Usage

Uses

Used in Flavoring and Perfumery Industry:
Benzaldehyde, 3-ethoxy-4-(1-methylethoxy)(9CI) is used as a flavoring agent for its almond-like aroma, enhancing the taste and scent of various food products and perfumes. Its unique odor profile makes it a valuable ingredient in creating appealing and distinctive flavors and fragrances.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, benzaldehyde, 3-ethoxy-4-(1-methylethoxy)(9CI) serves as a key component in the production of various medications. Its chemical properties allow it to be incorporated into drug formulations, contributing to the development of effective treatments for different health conditions.
Used as a Solvent in Organic Synthesis:
Benzaldehyde, 3-ethoxy-4-(1-methylethoxy)(9CI) is utilized as a solvent in organic synthesis processes. Its ability to dissolve a wide range of compounds makes it a versatile and valuable asset in chemical reactions, facilitating the synthesis of new compounds and materials.
Used in Antimicrobial and Insecticidal Applications:
Research has explored the potential antimicrobial and insecticidal properties of benzaldehyde, 3-ethoxy-4-(1-methylethoxy)(9CI). Its ability to inhibit the growth of microorganisms and deter insects could lead to its use in various applications, such as sanitizing products and pest control solutions.
However, it is crucial to handle benzaldehyde, 3-ethoxy-4-(1-methylethoxy)(9CI) with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken to minimize any potential risks associated with its use.

InChI:InChI=1/C12H16O3/c1-4-14-12-7-10(8-13)5-6-11(12)15-9(2)3/h5-9H,4H2,1-3H3

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 75-26-3 isopropyl bromide 
• 94-71-3 2-Ethoxyphenol 

Downstream Products

• 93475-29-7 3-Ethoxy-4-isopropyloxy-β-nitro-styrol 
• 284044-37-7 (4-isopropoxy-5-ethoxy-phenyl)-(4-cyano-phenylamino)-acetic acid methyl ester 
• 891842-07-2 (E)-4-(3-ethoxy-4-isopropoxybenzylideneamino)benzonitrile 
• 745020-14-8 2-amino-2-(3-ethoxy-4-isopropoxyphenyl)acetonitrile 
• 1448959-28-1 C₁₃H₁₇NO₃ 
• 745019-98-1 C₃₀H₂₇N₃O₆ 
• 745020-00-2 C₃₆H₃₂N₄O₇S 
• 745020-01-3 C₃₆H₃₂N₄O₇S 
• 745019-97-0 C₃₇H₃₃N₃O₆ 
• 745019-96-9 chloro-(3-ethoxy-4-isopropoxy-phenyl)-acetic acid benzyl ester 
• 745019-93-6 methyl 2-(3-ethoxy-4-isopropoxyphenyl)-2-hydroxyacetate 
• 745020-16-0 methyl 2-(3-ethoxy-4-isopropoxyphenyl)-2-(isoquinolin-6-ylamino)acetate 
• 745019-99-2 C₃₆H₃₂N₄O₇S 
• 745019-95-8 C₂₀H₂₄O₅ 

Relevant academic research and scientific papers

ISOINDOLE DERIVATIVE

Disclosed is a compound of formula (I) and a stereoisomer thereof: wherein R1, R2, R3 and R4 are as defined in the present disclosure.

Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium

The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.

N-(4- carbamimidoyl-phenyl) -glycine derivatives

The invention is concerned with novel N-(4-carbamimidoyl-phenyl)-glycine derivatives of the formula: wherein R1, E, X1 to X4 and G1 and G2 are as defined in the description and the claims, as well as hydrates or solvates and physiologically usable salts thereof.