30540-29-5 Usage
Uses
Used in Fragrance Industry:
2,3-Dimethylbutanoic acid methyl ester is used as a fragrance ingredient for its strong, fruity scent. It is incorporated into the production of perfumes and other consumer products to provide a pleasant and appealing aroma.
Used in Flavoring Industry:
In the flavoring industry, 2,3-Dimethylbutanoic acid methyl ester is used as a flavoring agent to impart a fruity taste to various food and beverage products, enhancing their overall flavor profile.
Used in Industrial Applications:
2,3-Dimethylbutanoic acid methyl ester is utilized as a solvent in various industrial processes. Its solvent properties make it suitable for use in the manufacturing of different products, including coatings, adhesives, and cleaning agents.
Safety Considerations:
Like other esters, 2,3-Dimethylbutanoic acid methyl ester is flammable, and therefore, it should be handled with caution to prevent any potential hazards. Proper safety measures and precautions should be taken during its storage, transportation, and use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 30540-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,4 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30540-29:
(7*3)+(6*0)+(5*5)+(4*4)+(3*0)+(2*2)+(1*9)=75
75 % 10 = 5
So 30540-29-5 is a valid CAS Registry Number.
30540-29-5Relevant academic research and scientific papers
Toward the development of efficient and stable Pd-catalysts for the methoxycarbonylation of medium chain alkenes
Bredenkamp, Tyler,Holzapfel, Cedric
, p. 421 - 427 (2016/01/27)
Methoxycarbonylation provides a one-step synthesis to valuable ester products utilised in both the fine and heavy chemical industry. However, in general, reaction rates for longer chain alkenes are poor which renders industrial implementation economical unviable. In cases where suitable rates are achieved, the requisite reagents are costly and in addition, the catalyst complexes readily decompose at elevated temperatures. This paper describes the use of an alternative ligand structural motif for the efficient methoxycarbonylation of terminal and internal medium chain alkenes to their corresponding esters. Promising results were obtained using a catalyst complex generated in situ from an unsymmetrical diphosphine ligand based on a ferrocene backbone, Pd(OAc)2 and methane sulfonic acid.
