34619-20-0 Usage
Description
1,4-Dibromo-2,3-dimethyl-2-butene is an organic compound characterized by its bromine atoms at the 1st and 4th carbon positions and methyl groups at the 2nd and 3rd carbon positions. It is a versatile reagent in chemical synthesis and analysis due to its unique structural features.
Uses
Used in Chemical Synthesis:
1,4-Dibromo-2,3-dimethyl-2-butene is used as a reagent for the synthesis of novel aldehyde and thiosemicarbazone derivatives. Its unique structure allows for the creation of a variety of complex organic molecules, which can be further utilized in various applications.
Used in Spectroscopic Characterization:
1,4-Dibromo-2,3-dimethyl-2-butene is also employed in the field of spectroscopy for the characterization of new aldehyde and thiosemicarbazone derivatives. Its distinct structural features make it an ideal candidate for studying the properties and interactions of these molecules through various spectroscopic techniques.
Used in Structural Studies:
1,4-Dibromo-2,3-dimethyl-2-butene is utilized in structural studies to understand the arrangement and conformation of novel aldehyde and thiosemicarbazone derivatives. This knowledge is crucial for predicting the behavior and potential applications of these compounds in various fields, such as pharmaceuticals, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 34619-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,1 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34619-20:
(7*3)+(6*4)+(5*6)+(4*1)+(3*9)+(2*2)+(1*0)=110
110 % 10 = 0
So 34619-20-0 is a valid CAS Registry Number.
34619-20-0Relevant articles and documents
Formal [5+1] annulation reactions of dielectrophilic peroxides: Facile access to functionalized dihydropyrans
Zhong, Chen,Yin, Qi,Zhao, Yukun,Li, Qinfeng,Hu, Lin
supporting information, p. 13189 - 13192 (2020/11/09)
A general [5+1] annulation reaction, which utilized 4-bromo- or 4-mesyloxy-but-2-enyl peroxides as unique five-atom bielectrophilic synthons to participate in the C-C and the subsequent umpolung C-O bond-forming reactions with C1 nucleophiles, has been developed for the facile synthesis of 2,2-disubstituted dihydropyrans in high yields under mild basic conditions. The dihydropyrans, which are readily prepared on a gram scale by this new method, can be flexibly transformed into the biologically important tetrahydropyrans and pyranones in 1-2 steps.
