632336-93-7 Usage
Derivative of butanone
It is a modified version of butanone This means that 1-Butanone, 2-bromo-1-(4-bromophenyl)is derived from the parent compound butanone by making structural modifications.
Contains bromine and phenyl groups
The presence of these functional groups in the molecule Bromine and phenyl groups are present in the chemical structure of 1-Butanone, 2-bromo-1-(4-bromophenyl)-, which contribute to its chemical reactivity and physical properties.
Used in organic synthesis
It serves as a building block for creating other compounds 1-Butanone, 2-bromo-1-(4-bromophenyl)is a valuable intermediate in the synthesis of various organic compounds.
Building block for pharmaceuticals and agrochemicals
It is utilized in the production of various medicines and pesticides This chemical compound is an important constituent in the manufacturing of a wide range of pharmaceutical and agrochemical products.
Employed as a reagent
It is used in research and industrial processes 1-Butanone, 2-bromo-1-(4-bromophenyl)is a useful reagent in various chemical reactions and processes, making it a common choice in both research and industrial settings.
Chemical and physical properties
The presence of bromine and phenyl groups influence its characteristics The bromine and phenyl groups in the molecule give 1-Butanone, 2-bromo-1-(4-bromophenyl)specific chemical and physical properties that make it suitable for a variety of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 632336-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,3,3 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 632336-93:
(8*6)+(7*3)+(6*2)+(5*3)+(4*3)+(3*6)+(2*9)+(1*3)=147
147 % 10 = 7
So 632336-93-7 is a valid CAS Registry Number.
632336-93-7Relevant academic research and scientific papers
Lu, Zheng,Yang, Yong-Qing
, p. 508 - 515 (2019)
Catalyst-free dehalogenation of α-haloketones under visible light irradiation is studied. The reactions were carried out in common organic solvent. The outcomes of dechlorination are excellent in yields up to 92%, and it is also applicable to bromides, which give even higher yields. The reaction is tolerable to a broad spectrum of substrates, especially to aromatic ketones, including various aryl and hetaryl groups. There are two examples of aliphatic ketones presented in the paper, although their reactivities are not as high as that of the aromatic ketones.
