889135-71-1 Usage
Uses
Used in the Food Industry:
(E)-3-(2-methoxy-5-methylphenyl)acrylaldehyde is used as a flavoring agent for its sweet, spicy, and floral aroma, enhancing the taste and smell of various food products.
Used in the Fragrance Industry:
In the fragrance industry, (E)-3-(2-methoxy-5-methylphenyl)acrylaldehyde is used as a key component in the production of perfumes, soaps, and other scented products, providing a unique and appealing scent.
Used in the Pharmaceutical Industry:
(E)-3-(2-methoxy-5-methylphenyl)acrylaldehyde is studied for its potential anti-inflammatory and antioxidant properties, making it a target for development in pharmaceutical applications.
Used in the Cosmetic Industry:
(E)-3-(2-methoxy-5-methylphenyl)acrylaldehyde is also being explored for its use in the cosmetic industry, where its anti-inflammatory and antioxidant properties could contribute to the development of skincare and other beauty products.
Check Digit Verification of cas no
The CAS Registry Mumber 889135-71-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,1,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 889135-71:
(8*8)+(7*8)+(6*9)+(5*1)+(4*3)+(3*5)+(2*7)+(1*1)=221
221 % 10 = 1
So 889135-71-1 is a valid CAS Registry Number.
889135-71-1Relevant academic research and scientific papers
Dehydrogenative β-Arylation of Saturated Aldehydes Using Transient Directing Groups
Zhang, Xing-Long,Pan, Gao-Fei,Zhu, Xue-Qing,Guo, Rui-Li,Gao, Ya-Ru,Wang, Yong-Qiang
supporting information, p. 2731 - 2735 (2019/04/30)
An unprecedented cross-dehydrogenative-coupling (CDC) reaction of saturated aldehyde β-C-H with arenes to form cinnamaldehydes via the cleavages of four C-H bonds has been developed. The reaction possesses complete E-stereoselectivity for the C=C double bond. The protocol is featured by atom and step economy, mild reaction conditions, and convenient operation.
Highly enantioselective 1,4-addition of arylzinc reagents to 3-arylpropenals catalyzed by a rhodium-binap complex in the presence of chlorotrimethylsilane
Tokunaga, Norihito,Hayashi, Tamio
, p. 607 - 613 (2007/10/03)
Asymmetric 1,4-addition of arylzinc chlorides to (E)-3-arylpropenals proceeded with high enantioselectivity in the presence of a rhodium/(R)-binap catalyst and chlorotrimethylsilane to give, after hydrolysis, high yields of the corresponding 3,3-diarylpro
