5398-02-7 Usage
Description
[(2-bromo-2-methylpropyl)sulfonyl]benzene is a chemical compound that features a benzene ring with a sulfonyl group and a 2-bromo-2-methylpropyl group attached to it. [(2-bromo-2-methylpropyl)sulfonyl]benzene is recognized for its utility in organic synthesis and its role as a versatile building block in the creation of a broad spectrum of organic molecules.
Uses
Used in Organic Synthesis:
[(2-bromo-2-methylpropyl)sulfonyl]benzene is used as a reagent for the introduction of the sulfonyl group into various organic molecules. Its unique structure allows for the formation of new compounds with potential applications in different fields.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, [(2-bromo-2-methylpropyl)sulfonyl]benzene serves as a precursor in the synthesis of various drugs. Its chemical properties make it a valuable component in the development of new medications.
Used in Agrochemical Synthesis:
Similarly, this compound is also utilized as a starting material in the production of agrochemicals, contributing to the development of substances that can be used in the agricultural sector for pest control and crop protection.
Used in Analytical Chemistry:
[(2-bromo-2-methylpropyl)sulfonyl]benzene is employed as a reference standard in analytical chemistry. It aids in the detection and quantification of sulfonyl compounds in various matrices, ensuring the accuracy and reliability of analytical results.
Check Digit Verification of cas no
The CAS Registry Mumber 5398-02-7 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 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5398-02:
(6*5)+(5*3)+(4*9)+(3*8)+(2*0)+(1*2)=107
107 % 10 = 7
So 5398-02-7 is a valid CAS Registry Number.
5398-02-7Relevant articles and documents
Methylenecyclopropanes in elimination and addition reactions: Quantification of the effects of strain
Volta, Luca,Stirling, Charles J. M.
experimental part, p. 1508 - 1522 (2010/03/24)
The effect of strain in 1,2-elimination reactions that form methylenecyclopropanes has been evaluated for a series of leaving groups. The worse the leaving group, the greater is the inhibitory effect of strain build-up, which reaches 50% of the excess enthalpy differential for the poorest leaving group studied. In nucleophilic addition to an electrophilic methylenecyclopropane, comparison of strained and unstrained systems shows that about 60% of the excess enthalpy differential promotes the reactivity of the strained system.
