5394-88-7 Usage
Description
1-(4-methoxy-3-methylphenyl)pentan-1-one, also known as p-Methoxy-α-methylpropyl phenylketone, is a chemical compound with the molecular formula C12H16O2. It is a ketone characterized by its carbonyl group (C=O) bonded to an alkyl group. 1-(4-methoxy-3-methylphenyl)pentan-1-one is a clear, colorless liquid with a sweet, floral odor and is soluble in organic solvents. It is considered to be low in toxicity and is used in various applications such as fragrances, flavorings, and as an intermediate for pharmaceutical products.
Uses
Used in Pharmaceutical Synthesis:
1-(4-methoxy-3-methylphenyl)pentan-1-one is used as an intermediate in the synthesis of pharmaceuticals for [application reason]. Its unique chemical structure allows it to be a valuable component in the development of new medications.
Used in Flavoring Agent for the Food Industry:
1-(4-methoxy-3-methylphenyl)pentan-1-one is used as a flavoring agent in the food industry for [application reason]. Its sweet, floral odor makes it a suitable candidate for enhancing the taste and aroma of various food products.
Used in Fragrances:
1-(4-methoxy-3-methylphenyl)pentan-1-one is used as a component in the fragrance industry for [application reason]. Its pleasant scent contributes to the creation of various perfumes, colognes, and other scented products.
Used in Organic Solvents:
1-(4-methoxy-3-methylphenyl)pentan-1-one is used in the formulation of organic solvents for [application reason]. Its solubility in organic solvents makes it a useful additive in various chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5394-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5394-88:
(6*5)+(5*3)+(4*9)+(3*4)+(2*8)+(1*8)=117
117 % 10 = 7
So 5394-88-7 is a valid CAS Registry Number.
5394-88-7Relevant articles and documents
Suzuki-Miyaura coupling of simple ketones via activation of unstrained carbon-carbon bonds
Xia, Ying,Wang, Jianchun,Dong, Guangbin
supporting information, p. 5347 - 5351 (2018/05/03)
Here, we describe that simple ketones can be efficiently employed as electrophiles in Suzuki-Miyaura coupling reactions via catalytic activation of unstrained C-C bonds. A range of common ketones, such as cyclopentanones, acetophenones, acetone and 1-indanones, could be directly coupled with various arylboronates in high site-selectivity, which offers a distinct entry to more functionalized aromatic ketones. Preliminary mechanistic study suggests that the ketone α-C-C bond was cleaved via oxidative addition.
An Efficient Catalytic Friedel-Crafts Acylation Reaction of Equimolar Amounts of Aromatic Compounds and Free Carboxylic Acids or Their Trimethylsilylesters via Mixes Anhydrides
Mukaiyama, Teruaki,Suzuki, Kaoru
, p. 1751 - 1754 (2007/10/02)
In the presence of an active catalyst generated from SiCl4 and AgClO4, the Friedel-Crafts acylation reaction between equimolar amount of aromatic compounds and mixed anhydrides, formed in situ from free carboxylic acids (or their trimethylsilylesters) and p-trifluoromethylbenzoic anhydride, smoothly proceeds at room temperatureto afford the corresponding aromatic ketones in high yields.
The Catalytic Friedel-Crafts Acylation Reaction Using a Catalyst Generated from GaCl3 and a Silver Salt
Mukaiyama, Teruaki,Ohno, Takashi,Nishimura, Takashi,Suda, Shinji,Kobayashi, Shu
, p. 1059 - 1062 (2007/10/02)
In the presence of a catalyst generated from GaCl3 and a silver salt (AgClO4 or AgSbF6), the Friedel-Crafts acylation reaction of aromatic compounds such as anisole and veratrole with acid anhydrides smoothly proceeds to afford the corresponding aromatic ketones in high yields.
