128405-69-6 Usage
Uses
Used in Organic Synthesis:
2-Hydroxyphenylcyclopropyl ketone is utilized as a building block in the synthesis of various pharmaceutical compounds, offering a versatile intermediate for the preparation of complex organic molecules. Its cyclopropyl group contributes to its unique reactivity, making it a valuable target for chemical research and development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-hydroxyphenylcyclopropyl ketone is employed as a key intermediate for the development of new pharmaceutical agents. Its structural features allow for the creation of diverse drug candidates with potential therapeutic applications.
Used in Fragrance Production:
2-Hydroxyphenylcyclopropyl ketone also finds use in the fragrance industry, where its unique aromatic properties can be harnessed to create novel scents and enhance existing fragrances.
Overall, 2-hydroxyphenylcyclopropyl ketone is a valuable and versatile chemical compound with wide-ranging potential applications in various industries, from pharmaceuticals to fragrances, underpinned by its distinctive chemical structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 128405-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,0 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 128405-69:
(8*1)+(7*2)+(6*8)+(5*4)+(4*0)+(3*5)+(2*6)+(1*9)=126
126 % 10 = 6
So 128405-69-6 is a valid CAS Registry Number.
128405-69-6Relevant articles and documents
Palladium-catalyzed ortho-CH-bond oxygenation of aromatic ketones
Choy, Pui Ying,Kwong, Fuk Yee
supporting information, p. 270 - 273 (2013/03/13)
A palladium-catalyzed C(sp2)-H bond oxygenation reaction is described. This protocol represents the first example of a C-H bond cleavage/C-O bond formation sequence, by employing a ketone moiety as the directing group. With this new catalytic method, a variety of ortho-acylphenols can be easily accessed from arylketones.
Preparation of Tetrahydrobenzindoles from 1-Tetralones
Beck, Anthony L.,Coates, William J.,Moody, Christopher J.
, p. 689 - 693 (2007/10/02)
3,4-Bridged indoles (5) are prepared from readily available aromatic ketones (1) by conversion into the epoxides (2), ring opening with azide ion to give the azido alcohols (3), dehydration, and thermolysis of the resulting vinyl azides (4).
