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(2Z)-3-ethoxybut-2-enoic acid, also known as (Z)-3-ethoxybut-2-enoic acid, is a chemical compound with the molecular formula C6H10O3. It is an unsaturated carboxylic acid with a butenoic acid structure and an ethoxy group, and it exists as a clear, colorless liquid.

38624-58-7

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38624-58-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(2Z)-3-ethoxybut-2-enoic acid is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Flavoring Agents:
In the food industry, (2Z)-3-ethoxybut-2-enoic acid is used as a flavoring agent to impart specific tastes and aromas to food products. Its ability to enhance flavors makes it a valuable ingredient in the development of new food products.
Used in Materials Science:
(2Z)-3-ethoxybut-2-enoic acid has potential applications in the field of materials science, particularly in the development of organic coatings and polymers. Its chemical properties can contribute to the creation of innovative materials with improved performance characteristics.
Used in Organic Coatings:
(2Z)-3-ethoxybut-2-enoic acid is used as a component in the formulation of organic coatings, providing properties such as adhesion, durability, and resistance to environmental factors. Its incorporation can lead to the development of advanced coating systems for various applications.
Used in Polymer Development:
In the field of polymer development, (2Z)-3-ethoxybut-2-enoic acid can be used to create new polymers with unique properties. Its presence in the polymer structure can enhance characteristics such as strength, flexibility, and chemical resistance, leading to the creation of innovative materials for various industries.
Safety and Handling:
It is important to handle (2Z)-3-ethoxybut-2-enoic acid with care, as it can cause skin and eye irritation. Proper protective equipment should be worn during its use, and it should be stored and disposed of responsibly to prevent environmental contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 38624-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,2 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38624-58:
(7*3)+(6*8)+(5*6)+(4*2)+(3*4)+(2*5)+(1*8)=137
137 % 10 = 7
So 38624-58-7 is a valid CAS Registry Number.

38624-58-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-ethoxybut-2-enoic acid

1.2 Other means of identification

Product number -
Other names 3-ethoxycrotonic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38624-58-7 SDS

38624-58-7Relevant academic research and scientific papers

Reaction of Methyl Anthranilate with Ethyl 3-Ethoxy-2-butenoyl Carbonate

Anand, R. C.,Sinha, A. K.

, p. 1043 - 1044 (2007/10/02)

Reaction of methyl anthranilate with ethyl 3-ethoxy-2-butenoyl carbonate affords 3-(2-carbomethoxyphenylamino)-2-butenoic acid (I) instead of the expected 3-ethoxy-2-buten-(2'-carbomethoxy)anilide (III).

Mevalonic acid analogs as inhibitors of cholesterol biosynthesis

DeBold,Elwood

, p. 1007 - 1010 (2007/10/02)

A series of 20 mevalonic acid analogs were synthesized and tested for their ability to inhibit cholesterol biosynthesis from [2-14C]-mevalonate in rat liver homogenates. Removal of the 5-hydroxyl group from mevalonic acid produced an active inhibitor, 3-hydroxy-3-methylpentanoic acid. Removal of the 3-hydroxyl group, addition of an aromatic group in the 3-position, or insertion of a double bond reduced inhibitory activity. Compounds with an aromatic group or halide on the 5-position were active inhibitors. The most active inhibitor was 5-phenylpentanoic acid, with 50% inhibition at 0.064 mM.

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