30957-25-6 Usage
Class
Ketones
This compound 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
This compound 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 this compound 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 articles and documents
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
