42050-06-6 Usage
Derived from phenanthrene
A derivative of phenanthrene, which is a polycyclic aromatic hydrocarbon, meaning it contains multiple carbon ring structures.
Phenanthrene core
Contains a core structure of phenanthrene, which is a significant feature of this chemical compound.
Carboxylic acid functional group
Has a carboxylic acid (-COOH) functional group attached to the phenanthrene core, giving it acidic properties.
Organic synthesis building block
Frequently used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals.
Potential anti-inflammatory properties
Has been studied for its potential to reduce inflammation, which could be beneficial in the development of anti-inflammatory drugs.
Potential anti-tumor properties
Also been studied for its potential to inhibit or prevent the growth of tumors, which could lead to the development of anti-tumor treatments.
Chelating agent
Utilized as a chelating agent to remove heavy metals from contaminated soil and wastewater, as it can form stable complexes with metal ions.
Production of dyes and pigments
Used in the manufacturing of dyes, pigments, and other chemical products due to its chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 42050-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42050-06:
(7*4)+(6*2)+(5*0)+(4*5)+(3*0)+(2*0)+(1*6)=66
66 % 10 = 6
So 42050-06-6 is a valid CAS Registry Number.
42050-06-6Relevant articles and documents
Synthesis and spectroscopy of nine isomeric methylacephenanthrylenes
Mulder, Patrick P. J.,Boere, Ben B.,Baart, Arthur,Cornelisse, Jan,Lugtenburg, Johan
, p. 22 - 32 (2007/10/02)
The synthesis of nine isomeric methyl-substituted acephenanthrylenes is described.Three different approaches were used. 1-, 2-, And 6-methylacephenanthrylene (1a, 1c and 1f) were prepared by formylation of acephenanthrene (2) and 4,5,7,8,9,10-hexahydroacephenanthrylene (17), followed by Wolff-Kishner reduction and dehydrogenation. 4-, 5-, 7- And 10-methylacephenanthrylene (1d, 1e, 1g and 1j) were synthesized by treating the corresponding acephenanthrenones with methyllithium, followed by dehydration and, in the case of 1g and 1j, dehydrogenation. 8- And 9-methylacephenanthrylene (1h and 1i) were prepared by a Haworth synthesis starting with the reaction of methylsuccinic anhydride with acenaphthene. the spectroscopic properties of acephenanthrylene and its methyl derivatives were investigated with mass spectrometry, (1)H NMR and UV-VIS spectroscopy.According to the (1)H NMR spectra, steric hindrance between the methyl group and nearby protons decreases in the following order: 1, 10 > 6 > 7 > 3 > 4, 5, 8, 9.
