98088-48-3 Usage
Description
(1-ALLYLOXY-BUT-3-ENYL)-BENZENE is a versatile chemical compound characterized by the presence of an allyloxy group connected to a but-3-enyl moiety, which is in turn attached to a benzene ring. This structure endows it with unique chemical reactivity and properties, making it a valuable building block in organic synthesis for the creation of a wide array of other compounds.
Uses
Used in Organic Synthesis:
(1-ALLYLOXY-BUT-3-ENYL)-BENZENE is used as a key building block for the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, such as chlorination, oxidation, and polymerization, which can lead to the formation of diverse derivatives with distinct chemical and physical properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1-ALLYLOXY-BUT-3-ENYL)-BENZENE is utilized as a precursor in the development of new drugs. Its ability to undergo multiple types of chemical reactions enables the creation of novel molecular structures with potential therapeutic applications.
Used in Chemical Research:
(1-ALLYLOXY-BUT-3-ENYL)-BENZENE serves as an important compound in chemical research, where it is studied for its reactivity and potential use in the development of new chemical processes and methodologies.
Used in Material Science:
In the field of material science, (1-ALLYLOXY-BUT-3-ENYL)-BENZENE is employed in the synthesis of new materials with specific properties. Its versatility in undergoing various reactions allows for the creation of materials with tailored characteristics for use in different applications.
Used in Specialty Chemicals Production:
(1-ALLYLOXY-BUT-3-ENYL)-BENZENE is used as a starting material in the production of specialty chemicals, which are often required for niche applications in various industries, such as agriculture, coatings, and fragrances. Its unique structure and reactivity contribute to the development of these high-value products.
Check Digit Verification of cas no
The CAS Registry Mumber 98088-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,8 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98088-48:
(7*9)+(6*8)+(5*0)+(4*8)+(3*8)+(2*4)+(1*8)=183
183 % 10 = 3
So 98088-48-3 is a valid CAS Registry Number.
98088-48-3Relevant articles and documents
Silylcyclopropanes by Selective [1,4]-Wittig Rearrangement of 4-Silyl-5,6-dihydropyrans
Mori-Quiroz, Luis M.,Maloba, Emmanuel W.,Maleczka, Robert E.
, p. 5724 - 5728 (2021/07/31)
4-Silyl-5,6-dihydropyrans undergo remarkably selective [1,4]-Wittig rearrangements to give silylcyclopropanes in good yields. The selectivity is independent of the silyl group, but it is influenced by the electronic character of the migrating center. Elec
Bronsted acid-catalyzed three-component hosomi-sakurai reactions
Kampen, Daniela,Ladepeche, Arnaud,Classen, Gerrit,Lista, Benjamin
experimental part, p. 962 - 966 (2009/05/27)
Aldehydes react with silyl ethers or the corresponding alcohols and allylsilanes in the presence of catalytic amounts of 2,4-dinitrobenzenesulfonic acid (DNBA) to provide a wide range of homoallylic ethers in moderate to high yields.
Trimethylsilyl trifluoromethanesulfonate catalyzed one-pot method for the conversion of aldehydes to homoallyl ethers in an ionic liquid
Anzalone, Peter W.,Mohan, Ram S.
, p. 2661 - 2663 (2007/10/03)
A mild method for the trimethylsilyl trifluoromethanesulfonate (TMSOTf) catalyzed one-pot synthesis of homoallyl ethers from aldehydes has been developed in the ionic liquid 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([bmim] [OTf]). The advanta
