4356-35-8 Usage
Class
Cycloheptatrienones
It belongs to a class of chemical compounds that contain a cycloheptatriene ring.
Cycloheptatriene ring
7-membered ring
The compound has a 7-membered carbon ring with alternating double bonds, known as a cycloheptatriene ring.
Hydroxyl groups
2
The compound contains two hydroxyl (-OH) groups, which are functional groups consisting of an oxygen atom bonded to a hydrogen atom.
Isopropyl group
1
The compound has one isopropyl (propan-2-yl) group attached to the cycloheptatriene ring, which is a 3-carbon alkyl group with the structure CH3-CH(CH3)-.
6. Synthetic organic compound
It is a man-made chemical compound, synthesized through chemical reactions, rather than being derived directly from natural sources.
7. Potential biological activity
The compound may have effects on biological systems, making it of interest for research and potential applications in pharmacology and medicine.
8. Pharmacological properties
It has properties that could be useful in the development of drugs or other treatments, and is studied for its possible effects on various biological processes.
9. Industrial applications
Due to its chemical reactivity and structure, the compound may have potential uses in various industrial processes or the production of other chemicals.
10. Research and medical studies
The compound is used in laboratory settings to study its properties, effects, and potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4356-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4356-35:
(6*4)+(5*3)+(4*5)+(3*6)+(2*3)+(1*5)=88
88 % 10 = 8
So 4356-35-8 is a valid CAS Registry Number.
4356-35-8Relevant 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.
The Palladium-mediated Cross-coupling of Bromotropolones with Organostannanes; Application to Concise Syntheses of β-Dolabrin, β-Thujaplicin, 7-Methoxy-4-isopropyltropolone, and β-Thujaplicinol
Banwell, Martin G.,Collis, Maree P.,Crisp, Geoffrey T.,Lambert, John N.,Reum, Monica E.,Scoble, Judith A.
, p. 616 - 617 (2007/10/02)
The bromotropolones (1), (2), and (3) cross-couple with organostannanes in the presence of palladium(O) to produce alkyl, alkenyl, or aryl substituted tropolones; the methodology has been applied to the synthesis of the monoterpenes β-dolabrin (4), β-thujaplicin (5), 7-methoxy-4-isopropyltropolone (7), and β-thujaplicinol (8).
