2606-54-4 Usage
Description
2-Hydroxymethylphenanthrene, also known as 2-hydroxy-1,2-dihydro-phenanthrein, is a white crystalline compound with the molecular formula C15H12O. It belongs to the phenanthrene family, which are polycyclic aromatic hydrocarbons (PAHs) commonly found in environmental and occupational settings. 2-HYDROXYMETHYLPHENANTHRENE is primarily used as a chemical intermediate for the synthesis of other organic compounds and has been a subject of studies investigating the potential health effects of exposure to PAHs, some of which are identified as potential carcinogens. Identified by the Chemical Abstracts Service (CAS) number 49016-26-6, further research is required to fully understand the potential risks and uses of 2-hydroxymethylphenanthrene.
Uses
Used in Chemical Synthesis Industry:
2-Hydroxymethylphenanthrene is used as a chemical intermediate for the synthesis of other organic compounds. Its unique structure and properties make it a valuable precursor in the production of various chemical products, contributing to the development of new materials and pharmaceuticals.
Used in Environmental and Occupational Health Research:
2-Hydroxymethylphenanthrene is utilized in research studies investigating the potential health effects of exposure to PAHs. As some PAHs have been identified as potential carcinogens, understanding the risks associated with 2-hydroxymethylphenanthrene can help in developing strategies to mitigate exposure and reduce health risks in various settings.
Check Digit Verification of cas no
The CAS Registry Mumber 2606-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2606-54:
(6*2)+(5*6)+(4*0)+(3*6)+(2*5)+(1*4)=74
74 % 10 = 4
So 2606-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O/c16-10-11-5-8-15-13(9-11)7-6-12-3-1-2-4-14(12)15/h1-9,16H,10H2
2606-54-4Relevant articles and documents
Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists
Morley, Richard M.,Tse, Heong-Wai,Feng, Bihua,Miller, Jacqueline C.,Monaghan, Daniel T.,Jane, David E.
, p. 2627 - 2637 (2007/10/03)
The binding site for competitive NMDA receptor antagonists is on the NR2 subunit, of which there are four types (NR2A-D). Typical antagonists such as (R)-AP5 have a subunit selectivity of NR2A > NR2B > NR2C > NR2D. The competitive NMDA receptor antagonist
AMINO-OXY-DERIVATIVES. V. SOME O-ETHERS OF 2-SUBSTITUTED
MAMALIS,GREEN,OUTRED,RIX
, p. 1829 - 1843 (2007/10/04)
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