134952-82-2 Usage
Uses
Used in Pharmaceutical Research:
2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxyis used as a key intermediate in the development of new drugs due to its potential to contribute to the creation of novel therapeutic agents with specific chemical and physical properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxyserves as a versatile building block for the synthesis of more complex molecules, facilitating the production of advanced organic compounds.
Used in Material Science:
2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxyis utilized in the production of novel materials with specific chemical and physical properties, potentially leading to innovations in various industries.
Used as a Reagent in Chemical Reactions:
2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxyalso functions as a reagent in various chemical reactions, playing a crucial role in the synthesis process and contributing to the formation of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 134952-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134952-82:
(8*1)+(7*3)+(6*4)+(5*9)+(4*5)+(3*2)+(2*8)+(1*2)=142
142 % 10 = 2
So 134952-82-2 is a valid CAS Registry Number.
134952-82-2Relevant academic research and scientific papers
The Palladium-Mediated Cross Coupling of Bromotropolones with Organostannanes or Arylboronic Acids: Applications to the Synthesis of Natural Products and Natural Product Analogues
Banwell, Martin G.,Cameron, Jennifer M.,Collis, Maree P.,Crisp, Geoffrey T.,Gable, Robert W.,'et al.
, p. 705 - 728 (2007/10/02)
The bromotropolones (4), (5) and (10) undergo palladium-mediated cross coupling with a wide range of organostannanes to produce alkenyl-, alkyl- and aryl-substituted tropolones.The methodology has been applied to the synthesis of the monoterpenes β-dolabrin (11), β-thujaplicin (12), 4-isopropyl-7-methoxytropolone (13) and β-thujaplicinol (14).Cross coupling of bromotropolones (4), (5) and (10) with various aryltrimethylstannanes or arylboronic acids has permitted the preparation of the bicyclic colchicine analogues (30)-(43) which have been tested for tubulin-binding activity.The X-ray crystal structure of the most active of these systems, compound (38), is reported.
