2549-50-0 Usage
Uses
Used in Plastics Industry:
Phenol,4,4'-(1,3-propanediyl)bisis used as a monomer in the production of polycarbonate plastics for its ability to create strong, lightweight, and transparent materials. These plastics are utilized in various applications, including automotive parts, compact discs, DVDs, and protective eyewear.
Used in Coatings Industry:
In the coatings industry, Phenol,4,4'-(1,3-propanediyl)bisis used as a component in epoxy resins, which are known for their excellent adhesion, chemical resistance, and mechanical properties. These resins are employed in coatings for automotive, aerospace, and marine applications, as well as in protective coatings for metal surfaces.
Used in Pharmaceutical Synthesis:
Phenol,4,4'-(1,3-propanediyl)bisis used as a precursor in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the development of new drugs and therapeutic agents, contributing to advancements in the medical field.
Used in Laboratory Research:
In laboratory settings, Phenol,4,4'-(1,3-propanediyl)bisis used as a research compound for studying its properties and potential applications. Researchers investigate its chemical behavior, reactivity, and interactions with other compounds to expand the knowledge of its possible uses and effects.
Check Digit Verification of cas no
The CAS Registry Mumber 2549-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2549-50:
(6*2)+(5*5)+(4*4)+(3*9)+(2*5)+(1*0)=90
90 % 10 = 0
So 2549-50-0 is a valid CAS Registry Number.
2549-50-0Relevant academic research and scientific papers
[...] compound and mesogenic medium
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Paragraph 0218; 0221, (2018/04/11)
wherein R11, R12, MG11, MG12 and CG1 have the meaning given in claim 1, to the use of bimesogenic compounds of formula I in liquid crystal media and particular to flexoelectric liquid crystal devices comprising a liquid crystal medium according to the pre
Understanding the reactivity of enol ether radical cations: Investigation of anodic four-membered carbon ring formation
Yamaguchi, Yusuke,Okada, Yohei,Chiba, Kazuhiro
, p. 2626 - 2638 (2013/04/23)
The reactivity of enol ether radical cations was investigated in anodic four-membered carbon ring formations, advancing the mechanistic understanding of these reactions. The mono-ring-containing aromatic cations were reduced through inter- or intramolecular electron transfer to give mono- or bis-ring-containing compounds, respectively. Small structural changes in the hydrocarbon linkers tethering two aromatic rings exerted a powerful effect on the efficiency of such electron transfer events.
SYNTHESIS OF ATR AND LIGHT SENSITIVE CIS-PHENOLIC CYCLOPROPANE DERIVATIVES
Afzal, Jalees,Magarian, Robert A.,Griffin, May,Pento, J. Thomas
, p. 3061 - 3068 (2007/10/02)
The synthesis of several cis-phenolic cyclopropanes, 6, 7, 8 and 13 is described.These cyclopropanes are new potential antiestrogens.A hydrogenolysis study of precursors, 5b, 5c, 5d, 10, 11, and 12, and a novel method for the prevention of gem-dichlorocyclopropane ring-opening during hydrogenolysis are discussed.
