17024-15-6 Usage
Chemical structure
A derivative of phenanthrene with a methyl group at the 10-position and a nitrile functional group at the 9-position.
Appearance
Typically a solid or crystalline substance.
Solubility
Soluble in organic solvents such as acetone, ethanol, and dichloromethane.
Stability
Relatively stable under normal conditions, but may decompose upon exposure to heat, light, or strong acids and bases.
Reactivity
Exhibits versatile reactivity due to the presence of the nitrile functional group, which can participate in various chemical reactions such as nucleophilic addition, hydrolysis, and reduction.
Organic synthesis
Used as a building block for the preparation of various organic compounds.
Pharmaceutical development
Potential applications in the development of pharmaceuticals due to its unique structural features.
Agrochemical development
Potential applications in the development of agrochemicals.
Industrial applications
May have potential in the production of dyes, pigments, and other fine chemicals.
Research interest
Attracts attention for its versatile reactivity and potential utility in various fields of chemistry, including organic synthesis, pharmaceuticals, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 17024-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17024-15:
(7*1)+(6*7)+(5*0)+(4*2)+(3*4)+(2*1)+(1*5)=76
76 % 10 = 6
So 17024-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H11N/c1-11-12-6-2-3-7-13(12)14-8-4-5-9-15(14)16(11)10-17/h2-9H,1H3
17024-15-6Relevant articles and documents
Stereoselective Protonation of Stable Carbanions Derived from 9,10-Dihydrophenanthrenes
Lewis, Frederick D.,Voe, Robert J. De
, p. 888 - 891 (1982)
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Synthesis of 9,10-Phenanthrenes via Palladium-Catalyzed Aryne Annulation by o-Halostyrenes and Formal Synthesis of (±)-Tylophorine
Yao, Tuanli,Zhang, Haiming,Zhao, Yanna
supporting information, p. 2532 - 2535 (2016/06/15)
A novel palladium-catalyzed annulation reaction of in situ generated arynes and o-halostyrenes has been developed. This methodology affords moderate to excellent yields of substituted phenanthrenes and is tolerant of a variety of functional groups such as nitrile, ester, amide, and ketone. This annulation chemistry has been successfully applied to the formal total synthesis of a biologically active alkaloid (±)-tylophorine.
