2510-70-5 Usage
Description
(9S,10S)-9,10-dihydrophenanthrene-9,10-dicarboxylic acid is a chemical compound with the molecular formula C16H14O4, belonging to the class of organic compounds known as polyaromatic compounds. Derived from polyaromatic hydrocarbons, it is a crystalline solid with a high melting point and is sparingly soluble in water.
Uses
Used in Organic Synthesis:
(9S,10S)-9,10-dihydrophenanthrene-9,10-dicarboxylic acid is used as a building block for the synthesis of more complex organic compounds, contributing to the development of novel chemical structures and functionalities.
Used in Material Science:
(9S,10S)-9,10-dihydrophenanthrene-9,10-dicarboxylic acid is used as a potential component in the field of material science, where its unique properties may be harnessed to create new materials with specific characteristics.
Used in Pharmaceutical Research:
(9S,10S)-9,10-dihydrophenanthrene-9,10-dicarboxylic acid is used as a potential candidate in pharmaceutical research, where its properties may be explored for the development of new drugs or drug delivery systems.
Further studies are needed to fully explore the potential uses and properties of (9S,10S)-9,10-dihydrophenanthrene-9,10-dicarboxylic acid in these and other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2510-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2510-70:
(6*2)+(5*5)+(4*1)+(3*0)+(2*7)+(1*0)=55
55 % 10 = 5
So 2510-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O4/c17-15(18)13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16(19)20/h1-8,13-14H,(H,17,18)(H,19,20)/t13-,14-/m1/s1
2510-70-5Relevant articles and documents
Reductive photocarboxylation of phenantnrene: A mechanistic investigation
Nikolaitchik, Alexander V.,Rodgers, Michael A. J.,Neckers, Douglas C.
, p. 1065 - 1072 (2007/10/03)
Irradiation of a solution of phenanthrene (PHN) in DMSO saturated with CO2 in the presence of N,N-dimethylaniline (DMA) produced 9,10-dihydrophenanthrene-9-carboxylic acid (1) in 55% yield, trans-9,10-dihydrophenanthrene-9,10-dicarboxylic acid (2) in 11% yield, a trace of phenanthrene-9-carboxylic acid (3), and a trace of 10-[p-(N,N-dimethylamino)phenyl]-9,10-dihydrophenanthrene-9-carboxylic acid (5). Addition of cumene, a hydrogen donor, or water, a proton donor, decreased the yield of 2, while addition of certain salts increased its yield. 9-Carboxy-9,10-dihydrophenanthr-10-yl, generated by irradiation of phenanthrene-9-carboxylic acid in the presence of DMA, is proposed to be an intermediate in the formation of the acids. The quantum yield for the formation of 2 increased to a maximum of 0.13 with increasing light intensity. High CO2 concentrations in DMSO changed the reaction pathway, greatly reducing the yields of 1 and 2, and phenanthrene-9-carboxylic acid (3) and 10-[p-(N,N-dimethylamino)phenyl]-9,10-dihydrophenanthrene-9-carboxylic acid (5) were formed instead. On the basis of these results reduction of 9-carboxy-9,10-dihydrophenanthr-10-yl with the phenanthrene radical anion is proposed to be a step in the mechanism accounting for trans-9,10-dihydrophenanthrene-9,10-dicarboxylic acid formation. Transient spectroscopic evidence in support of this proposal is presented.