4456-78-4 Usage
Description
1-(2,4,6-trimethylphenyl)prop-2-en-1-one, also known as p-methoxyphenylbenzaldehyde, is a chemical compound characterized by its molecular formula C10H12O. It is a yellow liquid with a strong, sweet, and intensely floral aroma, making it a valuable component in various industries due to its pleasant smell.
Uses
Used in Perfumery:
1-(2,4,6-trimethylphenyl)prop-2-en-1-one is used as a fragrance ingredient for its strong, sweet, and intensely floral aroma, contributing to the creation of various perfumes and colognes.
Used in Flavoring:
In the food and beverage industry, 1-(2,4,6-trimethylphenyl)prop-2-en-1-one is used as an additive to enhance the flavor of different products, capitalizing on its appealing scent.
Used in Pharmaceutical Synthesis:
1-(2,4,6-trimethylphenyl)prop-2-en-1-one is utilized as a key intermediate in the synthesis of various pharmaceuticals and organic compounds, playing a crucial role in the development of new medications.
Used in Agriculture:
1-(2,4,6-trimethylphenyl)prop-2-en-1-one has potential applications in agriculture, possibly serving as a component in the development of pest control agents or other agricultural chemicals.
Used in Food Preservation:
Its strong aroma and chemical properties make 1-(2,4,6-trimethylphenyl)prop-2-en-1-one a candidate for use in the food preservation industry, potentially aiding in the development of preservatives or additives that extend the shelf life of food products.
Safety Note:
It is important to handle 1-(2,4,6-trimethylphenyl)prop-2-en-1-one with care, as it can be irritant to the skin, eyes, and respiratory system. Proper safety measures should be taken during its use and production to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 4456-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4456-78:
(6*4)+(5*4)+(4*5)+(3*6)+(2*7)+(1*8)=104
104 % 10 = 4
So 4456-78-4 is a valid CAS Registry Number.
4456-78-4Relevant articles and documents
Nickel-Catalyzed C(sp3)-H Functionalization of Benzyl Nitriles: Direct Michael Addition to Terminal Vinyl Ketones
Zhang, Ninghui,Zhang, Chunli,Hu, Xiaoping,Xie, Xin,Liu, Yuanhong
supporting information, p. 6004 - 6009 (2021/07/31)
An efficient nickel(0)-catalyzed addition of benzyl nitriles to terminal vinyl ketones via C(sp3)-H functionalization has been developed. The reaction provides a novel and efficient protocol for the synthesis of α-functionalized benzyl nitriles with a wide range of structural diversity under mild reaction conditions while obviating the use of a strong base. The work might be potentially useful toward the development of an enantioselective variant using chiral nitrogen ligands.
Divergent stereocontrol of acid catalyzed intramolecular aldol reactions of 2,3,7-triketoesters: Synthesis of highly functionalized cyclopentanones
Truong, Phong,Shanahan, Charles S.,Doyle, Michael P.
supporting information; experimental part, p. 3608 - 3611 (2012/08/29)
The intramolecular acid catalyzed aldol cyclization of 2,3,7-triketoesters formed from Χ-keto-α-diazo-β-ketoesters provides highly functionalized cyclopentanones with good diastereoselectivity in high overall yields via kinetically controlled and stereodivergent catalytic processes. Lewis acid catalysis gives high selectivity for the 1,2-anti tetrasubstituted cyclopentanones, whereas Bronsted acid catalysis produces the corresponding 1,2-syn diastereomer.
