30957-25-6 Usage
Class
Ketones
2,6-Dimethyl-3,5-dibromo-4-heptanone belongs to the class of ketones, which are organic compounds containing a carbonyl group (C=O) bonded to two carbon atoms.
Structure
Two methyl groups, two bromine atoms, and a seven-carbon chain
The specific structure of 2,6-Dimethyl-3,5-dibromo-4-heptanone includes two methyl (CH3) groups, two bromine (Br) atoms, and a main chain of 7 carbon atoms.
Synthetic organic compound
It is a synthetic organic compound, meaning it is artificially created in a laboratory setting.
Building block in synthesis
The compound is commonly used as a building block in the synthesis of more complex organic molecules, aiding in the creation of a variety of chemical structures.
Reagent in chemical reactions
2,6-Dimethyl-3,5-dibromo-4-heptanone can be used as a reagent, meaning it plays an active role in chemical reactions, facilitating or enhancing the desired outcome.
Potential applications
Pharmaceutical, agrochemical, and other industries
2,6-Dimethyl-3,5-dibromo-4-heptanone has potential applications in various industries, including the development of pharmaceuticals and agrochemicals, due to its unique structure and reactivity.
Toxicity and handling precautions
2,6-Dimethyl-3,5-dibromo-4-heptanone is toxic, and it is essential to handle 2,6-Dimethyl-3,5-dibromo-4-heptanone with care to minimize health risks and ensure proper management.
Check Digit Verification of cas no
The CAS Registry Mumber 30957-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,5 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30957-25:
(7*3)+(6*0)+(5*9)+(4*5)+(3*7)+(2*2)+(1*5)=116
116 % 10 = 6
So 30957-25-6 is a valid CAS Registry Number.
30957-25-6Relevant academic research and scientific papers
Formation of α-iminoketones and α-diimines versus Favorskii rearrangement products from the reaction of α,α′-dibromoketones and primary amines
De Kimpe, Norbert,D'Hondt, Luc,Mones, Luc
, p. 3183 - 3208 (2007/10/02)
The reaction of aliphatic acyclic α,α'-dibromoketones with primary amines gave rise to α-iminoketones and α-diimines. Both reaction products could be selectively obtained under appropriate reaction conditions. Sterically hindered α,α-dibromoketones did no
