20291-73-0 Usage
Type of Compound
Polycyclic aromatic hydrocarbon (PAH)
Structure
A derivative of phenanthrene with two methyl groups attached at the 1 and 9 positions
Research laboratories
As a reference standard
Synthesis
Building block for more complex organic compounds
Medicinal Chemistry
Potential pharmacological and biological activities
Drug Discovery
Potential applications in developing new drugs
Environmental Concern
Potential environmental pollutant
Health Risk
Considered a potential carcinogen
Molecular Weight
228.32 g/mol (calculated from the chemical formula)
Physical State
Likely a solid at room temperature (typical for PAHs with similar molecular weight)
Appearance
Possibly a colorless or white crystalline solid (common for PAHs)
Solubility
Likely soluble in organic solvents such as acetone, ethanol, and benzene (typical for PAHs)
Melting Point
Not provided, but can be determined experimentally
Boiling Point
Not provided, but can be determined experimentally
Density
Not provided, but can be determined experimentally
Stability
Stable under normal temperature and pressure, but may decompose upon heating or exposure to light
Reactivity
May react with strong oxidizing agents, reducing agents, or under high temperature conditions
Hazardous Decompostion Products
Not provided, but could include toxic fumes or gases upon decomposition
Storage
Should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames
Disposal
Dispose of in accordance with local, national, and international regulations for hazardous chemicals
Check Digit Verification of cas no
The CAS Registry Mumber 20291-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,9 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20291-73:
(7*2)+(6*0)+(5*2)+(4*9)+(3*1)+(2*7)+(1*3)=80
80 % 10 = 0
So 20291-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H14/c1-11-6-5-9-15-14-8-4-3-7-13(14)12(2)10-16(11)15/h3-10H,1-2H3
20291-73-0Relevant academic research and scientific papers
Palladium-Catalyzed Sequential Vinyl C–H Activation/Dual Decarboxylation: Regioselective Synthesis of Phenanthrenes and Cyclohepta[1,2,3-de]naphthalenes
Jiang, Guomin,Ye, Hao,Shi, Lei,Dai, Hong,Wu, Xin-Xing
, p. 9398 - 9402 (2021/12/09)
The application of a C(vinyl), C(aryl)-palladacycle from vinyl-containing substrates is challenging due to the interference of a reactive double bond in palladium catalysis. This Letter describes a [4 + 2] or [4 + 3] cyclization based on a C(vinyl), C(aryl)-palladacycle by employing α-oxocarboxylic acids as the insertion units under a palladium/air system. The reaction proceeded through the key vinyl C–H activation and dual decarboxylation sequence, forming phenanthrenes and cyclohepta[1,2,3-de]naphthalenes regioselectively in good yields. The synthetic versatility of this protocol is highlighted by the gram-scale synthesis and synthesizing functional material molecule.
