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4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is a versatile research chemical compound characterized by its white or off-white powder or crystalline powder form and odorless nature. Its unique chemical structure, featuring a methacryloyloxy butoxy group attached to a benzene ring with a carboxylic acid group, makes it a valuable compound for various applications in scientific research and development.

92174-21-5

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92174-21-5 Usage

Uses

Used in Research and Development:
4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is used as a research chemical compound for its potential applications in various fields, including material science, pharmaceuticals, and chemical engineering. Its unique structure allows for further exploration and development of new compounds and materials with specific properties and functions.
Used in Material Science:
In the field of material science, 4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is used as a monomer or building block for the synthesis of polymers and copolymers with tailored properties. Its methacryloyloxy butoxy group enables copolymerization with other monomers, leading to the development of new materials with improved characteristics such as enhanced mechanical strength, thermal stability, and chemical resistance.
Used in Pharmaceutical Industry:
4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is used as an intermediate in the synthesis of pharmaceutical compounds, particularly those with potential therapeutic applications. Its unique structure can be modified or functionalized to create new drug candidates with specific biological activities, such as anti-inflammatory, analgesic, or antimicrobial properties.
Used in Chemical Engineering:
In chemical engineering, 4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is used as a reactant or catalyst in various chemical processes. Its carboxylic acid group can participate in esterification, amidation, or other condensation reactions, enabling the synthesis of new compounds or the modification of existing ones for specific applications.
Overall, 4-[4-(Methacryloyloxy)butoxy]benzenecarboxylic acid is a valuable research chemical compound with diverse applications in various industries, including material science, pharmaceuticals, and chemical engineering. Its unique structure and properties make it a promising candidate for further research and development to create new materials, drugs, and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 92174-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92174-21:
(7*9)+(6*2)+(5*1)+(4*7)+(3*4)+(2*2)+(1*1)=125
125 % 10 = 5
So 92174-21-5 is a valid CAS Registry Number.

92174-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-(2-methylprop-2-enoyloxy)butoxy]benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:92174-21-5 SDS

92174-21-5Relevant academic research and scientific papers

Process for the preparation of aromatic carboxylic acid

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Example 5, (2008/06/13)

A process for the preparation of an aromatic carboxylic acid comprises the steps of synthesizing a sulfonic ester having a (meth)acryloyloxy group by a reaction of a (meth)acrylic ester with a sulfonyl donor, synthesizing an aromatic aldehyde having a (meth)acryloyloxy group by a reaction of the sulfonic ester with an aromatic aldehyde and synthesizing an aromatic carboxylic acid by an oxidation of the aromatic aldehyde.

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