5919-69-7 Usage
Description
[(1Z)-3-ethoxyprop-1-en-1-yl]benzene, also known as 3-(1-phenylallyl)ethoxybenzene, is a chemical compound characterized by its molecular formula C11H14O. It is a colorless liquid with a strong, sweet odor. This versatile compound is valued for its applications across various industries due to its unique properties.
Uses
Used in the Food and Beverage Industry:
[(1Z)-3-ethoxyprop-1-en-1-yl]benzene is used as a flavoring agent for enhancing the taste and aroma of various food and beverage products. Its strong, sweet odor makes it a suitable candidate for creating appealing flavors in the culinary world.
Used in the Cosmetic and Personal Care Products Industry:
In the cosmetic and personal care sector, [(1Z)-3-ethoxyprop-1-en-1-yl]benzene serves as a fragrance component, adding a pleasant scent to products such as perfumes, lotions, and shampoos. Its sweet odor contributes to the overall sensory experience of these products.
Used in the Chemical Synthesis Industry:
[(1Z)-3-ethoxyprop-1-en-1-yl]benzene can also be utilized as an intermediate in the synthesis of other organic compounds. Its chemical structure allows for further reactions and modifications, making it a valuable building block in the creation of more complex molecules.
Safety Precautions:
It is important to handle [(1Z)-3-ethoxyprop-1-en-1-yl]benzene with care, as it has the potential to cause irritation to the skin, eyes, and respiratory system if not used properly. Appropriate safety measures should be taken to minimize the risk of exposure and ensure the well-being of those who work with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5919-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5919-69:
(6*5)+(5*9)+(4*1)+(3*9)+(2*6)+(1*9)=127
127 % 10 = 7
So 5919-69-7 is a valid CAS Registry Number.
5919-69-7Relevant articles and documents
Oxoammonium-Mediated Allylsilane–Ether Coupling Reaction
Carlet, Federica,Bertarini, Greta,Broggini, Gianluigi,Pradal, Alexandre,Poli, Giovanni
, p. 2162 - 2168 (2021/04/02)
A new C(sp3)?H functionalization reaction consisting of the oxidative α-allylation of allyl- and benzyl- methyl ethers has been developed. The C?C coupling could be carried out under mild conditions thanks to the use of cheap and green oxoammonium salts. The scope of the reaction was studied over 27 examples, considering the nature of the substituents on the two coupling partners.
Auto-Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones
Bakos, Mária,Gy?m?re, ádám,Domján, Attila,Soós, Tibor
supporting information, p. 5217 - 5221 (2017/04/27)
Herein we report that a single frustrated Lewis pair (FLP) catalyst can promote the reductive etherification of aldehydes and ketones. The reaction does not require an exogenous acid catalyst, but the combined action of FLP on H2, R-OH or H2O generates the required Br?nsted acid in a reversible, “turn on” manner. The method is not only a complementary metal-free reductive etherification, but also a niche procedure for ethers that would be either synthetically inconvenient or even intractable to access by alternative synthetic protocols.
Oxidative cleavage of allyl ethers by an oxoammonium salt
Kelly, Christopher B.,Ovian, John M.,Cywar, Robin M.,Gosselin, Taylor R.,Wiles, Rebecca J.,Leadbeater, Nicholas E.
, p. 4255 - 4259 (2015/04/14)
A method to oxidatively cleave allyl ethers to their corresponding aldehydes mediated by an oxoammonium salt is described. Using a biphasic solvent system and mild heating, cleavage proceeds readily, furnishing a variety of α,β-unsaturated aldehydes and ketones.
