27122-63-0 Usage
Description
[1-(allyloxy)ethyl]benzene is a chemical compound with the molecular formula C11H14O, characterized by a benzene ring attached to an ethyl group and an allyloxy group. [1-(allyloxy)ethyl]benzene is known for its reactivity due to the presence of the allyloxy group, which makes it a versatile building block in the synthesis of various organic compounds.
Uses
Used in Fragrance and Personal Care Industry:
[1-(allyloxy)ethyl]benzene is used as a key component in the fragrance and personal care industry, where it contributes to the development of scents and other formulations for products such as perfumes, lotions, and shampoos. Its unique chemical structure allows for the creation of diverse and complex fragrances.
Used in Organic Synthesis:
As a building block in organic synthesis, [1-(allyloxy)ethyl]benzene is used as a precursor for the production of various organic compounds. Its reactivity, particularly from the allyloxy group, facilitates the formation of new chemical bonds and the synthesis of a wide range of molecules.
Used in Pharmaceutical and Agrochemical Manufacturing:
[1-(allyloxy)ethyl]benzene is also utilized as a precursor in the manufacture of pharmaceuticals and agrochemicals. Its reactivity and structural properties make it a valuable starting material for the development of new drugs and agricultural chemicals.
Used in the Food Industry:
[1-(allyloxy)ethyl]benzene serves as a flavoring agent in the food industry, where it is used to enhance the taste and aroma of various products. Its unique chemical structure allows for the creation of distinct and appealing flavors.
Safety Precautions:
It is important to handle [1-(allyloxy)ethyl]benzene with care, as it may pose health risks and is flammable. Proper safety measures should be taken during its use and storage to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 27122-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27122-63:
(7*2)+(6*7)+(5*1)+(4*2)+(3*2)+(2*6)+(1*3)=90
90 % 10 = 0
So 27122-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O/c1-3-9-12-10(2)11-7-5-4-6-8-11/h3-8,10H,1,9H2,2H3
27122-63-0Relevant articles and documents
Addition of alcohols and acids to olefins in presence of zeolite catalyst H-beta
Raskildina, Gulnara Z.,Kazakova, Anna N.,Mikhailova, Natalia N.,Grigor'Eva, Nelly G.,Kutepov, Boris I.,Zlotsky, Simon S.
, p. 811 - 815 (2015/06/30)
By studying the reactions of styrene and norbornene with different alcohols and carbonic acids in the presence of heterogenic catalyst, it was found that the selected zeolite H-Beta is an active and selective catalyst for these reactions. Ethers and esters of norbornene have exo-configuration. It has been established that reaction of norbornene with diols, catalyzing by zeolite Beta, leads to the formation of esters, which have not been found before.
Facile and selective deallylation of allyl ethers using diphosphinidenecyclobutene-coordinated palladium catalysts
Murakami, Hiromi,Minami, Tatsuya,Ozawa, Fumiyuki
, p. 4482 - 4486 (2007/10/03)
(π-Allyl)palladium triflate bearing a 1,2-bis(4-methoxyphenyl)-3,4- bis(2,4,6-tri-tert-butylphenylphosphinidene)cyclobutene ligand (DPCB-OMe), [Pd(η3-C3H5)(DPCB-OMe)]OTf, efficiently catalyzes deallylation of a variety of allyl ethers in aniline to give corresponding alcohols in high yields under mild conditions. The reactions can be performed in air without loss of a variety of functionalities including vinyl, alkynyl, hydroxy, acetoxy, silyloxy, and acetal groups. Allyl 2-allyloxybenzoate selectively undergoes deallylation of the allyloxy group to give allyl salicylate in quantitative yield.
Efficient reductive etherification of carbonyl compounds with alkoxytrimethylsilanes
Hatakeyama, Susumi,Mori, Hisato,Kitano, Kaori,Yamada, Hidetoshi,Nishizawa, Mugio
, p. 4367 - 4370 (2007/10/02)
An efficient TMSOTf catalyzed ether synthesis from carbonyl compounds and alkoxytrimethylsilanes via triethylsilane-reduction is described.
