53403-90-0 Usage
Uses
Used in Perfumery:
(E)-1-Phenyl-hept-3-en-1-one is used as a fragrance ingredient for its distinct floral scent, contributing to the creation of various perfumes and colognes.
Used in Flavoring Industry:
In the food and beverage industry, (E)-1-Phenyl-hept-3-en-1-one is used as a flavoring agent to enhance the taste and aroma of different products.
Used in Organic Synthesis:
(E)-1-Phenyl-hept-3-en-1-one serves as a building block in the synthesis of various organic compounds, playing a significant role in the development of new chemical entities.
Used in Essential Oils:
(E)-1-PHENYL-HEPT-3-EN-1-ONE is often found in essential oils, where it contributes to the overall scent and therapeutic properties of the oil.
Used in Antimicrobial Applications:
(E)-1-Phenyl-hept-3-en-1-one has been studied for its antimicrobial properties, which may find use in the development of new antimicrobial agents.
Used in Antioxidant Applications:
The antioxidant properties of (E)-1-Phenyl-hept-3-en-1-one have potential applications in the pharmaceutical and cosmetic industries, where antioxidants are highly valued for their ability to protect cells from damage caused by free radicals.
Check Digit Verification of cas no
The CAS Registry Mumber 53403-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,0 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53403-90:
(7*5)+(6*3)+(5*4)+(4*0)+(3*3)+(2*9)+(1*0)=100
100 % 10 = 0
So 53403-90-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O/c1-2-3-4-8-11-13(14)12-9-6-5-7-10-12/h4-10H,2-3,11H2,1H3/b8-4+
53403-90-0Relevant academic research and scientific papers
Rearrangement of allylic and propargylic alcohols catalyzed by the combined use of tetrabutylammonium perrhenate(VII) and p-toluenesulfonic acid
Narasaka,Kusama,Hayashi
, p. 2059 - 2068 (2007/10/02)
Allylic rearrangement and/or dehydration reaction of allylic alcohols proceeds smoothly by the use of catalytic amounts of tetrabutylammonium perrhenate and p-toluenesulfonic acid hydrate. Treatment of propargylic alcohols with the catalysts at room temperature affords the rearranged products, α,β-unsaturated carbonyl compounds, while β,γ-unsaturated ketones are obtained as main products by the reaction in refluxing 1,2-dichloroethane. The application of this catalytic system is also described for the preparation of some synthetic intermediates.
ISOMERAZATION OF PROPARGYLIC ALCOHOLS CATALYZED BY AN IRIDIUM COMPLEX
Ma, Dawei,Lu, Xiyan
, p. 2109 - 2112 (2007/10/02)
α,β-Enones were synthesized by the isomerization of propargylic alcohols catalyzed by an iridium pentahydride complex.
