473255-19-5 Usage
Uses
Used in Coordination Chemistry and Metal Complexation:
1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)is used as a ligand for chelation of metal ions in coordination chemistry. Its ability to form stable complexes with metal ions makes it a crucial component in the study and development of new coordination compounds.
Used in Organic Electronic Devices:
In the field of organic electronics, 1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)is utilized as a component in the development of electronic devices due to its favorable properties, such as its compatibility with other organic materials and its ability to enhance device performance.
Used as a Surfactant:
The octyloxy groups present in the compound make 1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)suitable for use as a surfactant in various applications. Its surfactant properties can be harnessed in industries such as pharmaceuticals, cosmetics, and cleaning products to improve the solubility, stability, and efficacy of formulations.
Used in Materials Science:
The unique structure and properties of 1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)make it a valuable compound in materials science. It can be used to develop new materials with specific properties, such as improved conductivity, stability, or reactivity, which can be applied in various technological advancements.
Used in Chemical Synthesis:
As a complex organic compound, 1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)can be employed in chemical synthesis to create new molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Catalysis:
1,10-Phenanthroline, 3,8-dibromo-5,6-bis(octyloxy)-'s ability to chelate metal ions also makes it a useful catalyst or catalyst precursor in various chemical reactions. It can be employed to improve the efficiency and selectivity of catalytic processes, leading to more sustainable and cost-effective production methods in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 473255-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,2,5 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 473255-19:
(8*4)+(7*7)+(6*3)+(5*2)+(4*5)+(3*5)+(2*1)+(1*9)=155
155 % 10 = 5
So 473255-19-5 is a valid CAS Registry Number.
473255-19-5Relevant academic research and scientific papers
Yamamoto, Takakazu,Anzai, Kazushige,Fukumoto, Hiroki
, p. 774 - 775 (2002)
Soluble π-conjugated poly(dialkoxyphenanthroline)s were prepared by organometallic polycondensation using a Ni(0) complex. Stacking structure, optical and electrochemical properties, and Ru complex forming reactivity of the polymer have been revealed.
Yamamoto, Takakazu,Saitoh, Yutaka,Anzai, Kazushige,Fukumoto, Hiroki,Yasuda, Takuma,Fujiwara, Yoshiki,Choi, Byoung-Ki,Kubota, Kenji,Miyamae, Takayuki
, p. 6722 - 6729 (2003)
π-Conjugated poly(1,10-phenanthroline-3,8-diyl), PPhen, and its 5,6-dialkoxy derivatives. PPhen(5,6-OR)s, have been synthesized by using an organometallic polycondensation with a zerovalent nickel complex. They have average molecular weights of 4300-6800. PPhen had a stiff structure, as revealed by a light scattering method, and exhibited a strong dichroism in UV-vis absorption and photoluminescence. PPhen(5,6-OR)s formed an end-to-end packing assembly assisted by the side chain crystallization of the OR groups. PPhen and PPhen(5,6-OR)s were susceptible to chemical and electrochemical reduction, and the reduced state showed certain stability toward oxygen in air. The π-conjugated polymers underwent quantitative complex formation with [Ru(bpy)2]2+. Introduction of two more imine nitrogens in the repeating unit of PPhen enhanced much the electron accepting property of PPhen, and n-doping of the obtained polymer took place at Epc of -1.38 V vs Ag+/Ag.
