78500-90-0 Usage
Uses
Used in Chemical Research and Development:
(2,6-diphenyl-4-pyridyl)-(2-nitrophenyl)methanol serves as a valuable compound in the field of chemical research and development. Its unique structure, which includes multiple aromatic rings and a nitro group, makes it a candidate for exploring novel chemical reactions and properties. Researchers may utilize (2,6-diphenyl-4-pyridyl)-(2-nitrophenyl)methanol to investigate its reactivity, stability, and potential applications in the synthesis of new materials or pharmaceutical agents.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2,6-diphenyl-4-pyridyl)-(2-nitrophenyl)methanol may be employed as an intermediate or a building block in the synthesis of various drug molecules. Its complex structure and functional groups could be leveraged to create new compounds with specific therapeutic effects or to improve the pharmacokinetic properties of existing drugs.
Used in Material Science:
(2,6-diphenyl-4-pyridyl)-(2-nitrophenyl)methanol could also find applications in material science, particularly in the development of new polymers, coatings, or composite materials. (2,6-diphenyl-4-pyridyl)-(2-nitrophenyl)methanol's aromatic and potentially reactive nature may contribute to the creation of materials with unique mechanical, thermal, or optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 78500-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78500-90:
(7*7)+(6*8)+(5*5)+(4*0)+(3*0)+(2*9)+(1*0)=140
140 % 10 = 0
So 78500-90-0 is a valid CAS Registry Number.
78500-90-0Relevant academic research and scientific papers
Intramolecular Nitrene Insertions into Aromatic and Heteroaromatic Systems. Part 7. Insertions into Electron-deficient Rings
Carde, Robert N.,Hayes, Peter C.,Jones, Gurnos,Cliff, Cynthya J.
, p. 1132 - 1142 (2007/10/02)
A number of routes to o-aminotriphenylmethanes are described, where one benzene ring, or both, carry potential ester groups.The most useful synthon is shown to be the 1,3-dioxan-2-yl substituent, and using this methyl 2-aminodiphenylmethane-4'-carboxylate (18) and dimethyl 2-aminotriphenylmethane-4',4''-dicarboxylate (28) have been prepared.The azides from these, respectively (19) and (29), on thermolysis at 200 deg C gave azepinoindoles (48) and (51), the first examples of ring expansion by an arylnitrene of benzene rings with electron-withdrawing substituents.Also reported are syntheses of 3- and 4-(2-azidobenzyl)pyridines (38) and (39), and of 2-(2-azidobenzyl)thiazole (40); decomposition of these azides gave mainly polymers.
