16004-91-4 Usage
Uses
Used in Organic Synthesis:
2-Cyclohexen-1-one, 4-bromo-3,5,5-trimethylis used as a building block in organic synthesis for the creation of various compounds. Its unique structure and functional groups make it a valuable intermediate in the synthesis of complex organic molecules.
Used in Chemical Research:
In the field of chemical research, 2-Cyclohexen-1-one, 4-bromo-3,5,5-trimethylserves as a reagent for studying the properties and reactions of brominated cyclohexenones. Researchers utilize 2-Cyclohexen-1-one, 4-bromo-3,5,5-trimethyl- to explore its reactivity, stability, and potential applications in the development of new chemical processes and materials.
Used in Laboratory Experiments:
2-Cyclohexen-1-one, 4-bromo-3,5,5-trimethylis also employed as a reagent in laboratory experiments. It is used to test various chemical reactions, assess the effects of bromination on cyclohexenone derivatives, and investigate the influence of methyl group substitution on the compound's properties.
While the provided materials do not explicitly mention any specific industrial applications or biological activities of 2-Cyclohexen-1-one, 4-bromo-3,5,5-trimethyl-, its use in organic synthesis, chemical research, and laboratory experiments highlights its potential for further exploration and development in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 16004-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,0 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16004-91:
(7*1)+(6*6)+(5*0)+(4*0)+(3*4)+(2*9)+(1*1)=74
74 % 10 = 4
So 16004-91-4 is a valid CAS Registry Number.
16004-91-4Relevant academic research and scientific papers
Oxidation of α,β-enones and alkenes with oxone and sodium halides: A convenient laboratory preparation of chlorine and bromine
Dieter, R. Karl,Nice, Lois E.,Velu, Sadanandan E.
, p. 2377 - 2380 (2007/10/03)
Mixtures of oxone and sodium chloride or sodium bromide afford solutions of chlorine or bromine, respectively. These solutions effectively add chlorine and bromine to α,β-enones and alkenes. The method affords improved yields of 3-alkyl-2-halo-2-cycloalkenones which are sometimes difficult to prepare.
THE ALLYLIC REARRANGEMENT. V. REACTION OF 4-HALOISOPHORONE WITH SODIUM METHOXIDE IN METHANOL
Tsuboi, Sadao,Kurihara, Yoichi,Watanabe, Takayuki,Takeda, Akira
, p. 773 - 780 (2007/10/02)
Treatment of 4-bromoisophorone with sodium methoxide gave 2-methoxyisophorone (4).Reaction of 4-chloroisophorone with sodium methoxide at 65-70 deg C afforded Favorskii-type rearrangement product along with 4.
