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(S)-methyl 2-(4-butylphenyl)propanoate, with the molecular formula C13H18O2, is a chemical compound belonging to the ester class. It is formed through the reaction between an alcohol and an acid. (S)-methyl 2-(4-butylphenyl)propanoate is recognized for its pleasant odor and has been studied for its potential biological activities, such as anti-inflammatory and antioxidant properties.

404354-75-2

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404354-75-2 Usage

Uses

Used in Perfumery and Fragrance Industry:
(S)-methyl 2-(4-butylphenyl)propanoate is used as a key ingredient in the creation of perfumes and fragrances, leveraging its appealing scent to enhance the overall aroma of these products.
Used in Flavor and Food Industry:
In addition to its application in perfumes and fragrances, (S)-methyl 2-(4-butylphenyl)propanoate is also utilized as a flavoring agent in the food and beverage sector, adding a distinct taste and aroma to various products.
Used in Pharmaceutical Research:
(S)-methyl 2-(4-butylphenyl)propanoate is studied for its potential biological activities, including its role as an anti-inflammatory and antioxidant agent. This research could lead to the development of new pharmaceutical applications for this versatile chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 404354-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,5 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 404354-75:
(8*4)+(7*0)+(6*4)+(5*3)+(4*5)+(3*4)+(2*7)+(1*5)=122
122 % 10 = 2
So 404354-75-2 is a valid CAS Registry Number.

404354-75-2Upstream product

404354-75-2Relevant academic research and scientific papers

Synthesis of new chiral dopants derived from 2-phenylpropanoic acid derivatives for nematic liquid crystals

Aoki, Yoshio,Shitara, Hiroaki,Hirose, Takuji,Nohira, Hiroyuki

, p. 2219 - 2222 (2007/10/03)

New chiral dopants for nematic liquid crystals were synthesized using optically active 2-phenylpropanoic acid derivatives. The magnitude of the helical twisting power (HTP) was largely influenced by the terminal group of the asymmetric frame and the core

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