136944-08-6 Usage
Chemical structure
A conjugated enone containing a benzodioxole ring and a dimethoxyphenyl group.
Potential pharmaceutical applications
The compound has been studied for its potential anti-inflammatory, analgesic, and anti-cancer properties.
Enzyme inhibition
It is believed to have the ability to inhibit certain enzymes, which could contribute to its potential therapeutic uses.
Cellular signaling modulation
The compound may modulate cellular signaling pathways, which could be relevant for its potential pharmaceutical applications.
Further research needed
More research is required to fully understand the biological activity and potential therapeutic uses of this chemical compound.
Molecular weight
Approximately 314.30 g/mol
Appearance
The compound is likely to be a solid, with a molecular structure that may exhibit a planar or slightly twisted conformation due to the presence of the conjugated enone system and the aromatic rings.
Solubility
The compound may have varying solubility in different solvents, with potential solubility in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO), depending on the specific functional groups and their interactions.
Stability
The stability of the compound may depend on factors such as temperature, light exposure, and the presence of other reactive substances. It is important to store and handle the compound according to appropriate guidelines to maintain its integrity and potential therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 136944-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136944-08:
(8*1)+(7*3)+(6*6)+(5*9)+(4*4)+(3*4)+(2*0)+(1*8)=146
146 % 10 = 6
So 136944-08-6 is a valid CAS Registry Number.
136944-08-6Relevant academic research and scientific papers
Synthesis of highly functionalized 9,10-phenanthrenequinones by oxidative coupling using MoCl5
Trosien, Simon,Waldvogel, Siegfried R.
supporting information; experimental part, p. 2976 - 2979 (2012/07/27)
The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular fashion and in excellent yields. By this approach the orchid-derived natural product cypripediquinone A was synthesized for the first time.
Synthesis of unsymmetrically substituted benzils via the Friedel-Crafts reaction of arenes with α-chloro-α-(methylthio)acetophenones
Ishibashi,Matsuoka,Ikeda
, p. 1854 - 1856 (2007/10/02)
Lewis acid-promoted reactions of arenes with α-chloro-α-(methylthio)acetophenones gave the Friedel-Crafts reaction products, which were then treated with 3 molar eq of cupric chloride in aqueous acetone to afford the unsymmetrically substituted benzils.
