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Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is a chemical compound with the molecular formula C10H11NO3. It is an ester derivative of benzoic acid, characterized by the presence of a cyanomethyl and methoxy group. Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is known for its versatile applications in various industries, including the production of fragrances, flavors, pharmaceuticals, and as a preservative due to its antimicrobial properties.

24550-59-2

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24550-59-2 Usage

Uses

Used in Fragrance and Flavor Industry:
Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is used as a key ingredient in the creation of various fragrances and flavors. Its unique chemical structure imparts a distinct aroma and taste, making it a valuable component in the formulation of perfumes, colognes, and food products.
Used in Pharmaceutical Industry:
Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester serves as an intermediate in the synthesis of various pharmaceuticals. Its ability to be modified and combined with other molecules allows for the development of new drugs with potential therapeutic effects.
Used as a Preservative:
Due to its antimicrobial properties, benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is used as a preservative in a wide range of products. It helps to prevent the growth of bacteria, mold, and yeast, thereby extending the shelf life of products and maintaining their quality.
Used in the Synthesis of Organic Compounds:
Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is utilized in the synthesis of other organic compounds, contributing to the development of new materials and chemical products.
Used in Dye and Pigment Production:
Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester is also used as an intermediate in the production of dyes and pigments, playing a crucial role in the creation of vibrant colors for various applications.
Used in Therapeutic Research:
Benzoic acid, 5-(cyanomethyl)-2-methoxy-, methyl ester has been studied for its potential therapeutic effects in the treatment of various medical conditions. Its unique properties and ability to interact with biological systems make it a promising candidate for further research and development in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 24550-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24550-59:
(7*2)+(6*4)+(5*5)+(4*5)+(3*0)+(2*5)+(1*9)=102
102 % 10 = 2
So 24550-59-2 is a valid CAS Registry Number.

24550-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-(cyanomethyl)-2-methoxybenzoate

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:24550-59-2 SDS

24550-59-2Relevant academic research and scientific papers

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: Novel human PPARα-selective activators

Miyachi, Hiroyuki,Nomura, Masahiro,Tanase, Takahiro,Takahashi, Yukie,Ide, Tomohiro,Tsunoda, Masaki,Murakami, Koji,Awano, Katsuya

, p. 77 - 80 (2007/10/03)

A series of substituted phenylpropanoic acid derivatives was prepared as part of a search for subtype-selective human peroxisome proliferator-activated receptor (PPAR) activators. Structure-activity relationship studies indicated that the substituent at the α-position of the carboxyl group plays a key role in determining the potency and the selectivity for PPAR transactivation.

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