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(3-ethoxy-phenyl)-acetaldehyde is a chemical compound belonging to the aldehyde family, with the molecular formula C10H12O2. It features a carbonyl group (C=O) bonded to a hydrogen atom and an aromatic ring with an ethoxy group (C2H5O) attached to it. (3-ethoxy-phenyl)-acetaldehyde is known for its aromatic nature and is utilized in various applications across the chemical and pharmaceutical industries.

433229-41-5

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433229-41-5 Usage

Uses

Used in Organic Synthesis:
(3-ethoxy-phenyl)-acetaldehyde is used as a building block in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows it to be a versatile component in the creation of a wide range of compounds.
Used in Flavor and Fragrance Industry:
Due to its aromatic properties, (3-ethoxy-phenyl)-acetaldehyde is used as a flavor and fragrance ingredient. It contributes to the development of scents and tastes in various consumer products, enhancing the sensory experience.
Used in Antifungal and Antibacterial Applications:
(3-ethoxy-phenyl)-acetaldehyde has been studied for its potential biological activities, including its role as an antifungal and antibacterial agent. This makes it a candidate for use in applications where control of microbial growth is necessary, such as in medical or environmental settings.

Check Digit Verification of cas no

The CAS Registry Mumber 433229-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,2,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 433229-41:
(8*4)+(7*3)+(6*3)+(5*2)+(4*2)+(3*9)+(2*4)+(1*1)=125
125 % 10 = 5
So 433229-41-5 is a valid CAS Registry Number.

433229-41-5Downstream Products

433229-41-5Relevant academic research and scientific papers

Synthesis of bruguierol A employing ring closing metathesis

Sarkar, Debayan,Venkateswaran, Ramanathapuram V.

, p. 3232 - 3233 (2011)

An expedient synthesis of bruguierol A encompassing a novel 2,3-benzo-8-oxabicyclo[3.2.1]octane ring system is described employing ring closing metathesis to generate the oxa-bridged tricyclic core.

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