134952-82-2 Usage
General Description
2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxy- is a chemical compound with a complex molecular structure. It consists of a seven-membered carbon ring with a ketone group at one end and two methoxy groups attached to a phenyl ring at the other end. 2,4,6-Cycloheptatrien-1-one, 5-(2,4-dimethoxyphenyl)-2-methoxy- is often used in organic synthesis and pharmaceutical research due to its unique aromatic and functional properties. It has potential applications in the development of new drugs, as well as in the production of novel materials with specific chemical and physical properties. Additionally, it may also be used as a reagent in chemical reactions and as a building block in the synthesis of more complex molecules.
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 articles and documents
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.
