85390-98-3 Usage
Description
[1,1':3',1''-Terphenyl]-2'-carboxaldehyde, 5'-phenylis a complex chemical compound characterized by its three phenyl rings and a carboxaldehyde group. It is classified as an aldehyde and is known for its high stability and reactivity, making it a versatile building block in organic synthesis. The phenyl group in its structure contributes to its aromatic and hydrophobic properties, which are beneficial in the development of materials and compounds with specific characteristics.
Uses
Used in Pharmaceutical Industry:
[1,1':3',1''-Terphenyl]-2'-carboxaldehyde, 5'-phenylis used as an intermediate in the synthesis of various pharmaceuticals due to its reactivity and stability. Its unique structure allows for the creation of new drugs with specific properties and functions.
Used in Dye Industry:
In the dye industry, [1,1':3',1''-Terphenyl]-2'-carboxaldehyde, 5'-phenylis used as a starting material for the production of dyes with specific color properties. Its aromatic nature contributes to the development of dyes with enhanced color intensity and stability.
Used in Specialty Chemicals:
[1,1':3',1''-Terphenyl]-2'-carboxaldehyde, 5'-phenylis also utilized in the production of specialty chemicals, where its unique structure and properties are harnessed to create compounds with specific applications in various industries, such as materials science and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 85390-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,9 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85390-98:
(7*8)+(6*5)+(5*3)+(4*9)+(3*0)+(2*9)+(1*8)=163
163 % 10 = 3
So 85390-98-3 is a valid CAS Registry Number.
85390-98-3Relevant articles and documents
Synthesis and structural characterization of m-terphenyl Schiff base ligands and their aluminum complexes
Dickie, Diane A.,Jalali, Hanifa,Samant, Rahul G.,Jennings, Michael C.,Clyburne, Jason A.C.
, p. 1346 - 1352 (2007/10/03)
2,4,6-Triphenylbenzaldehyde 1 undergoes a condensation reaction with 2-aminophenol to give N-(2′,4′,6′-triphenylbenzylidene)-2- iminophenol (TPIP) 2. The imine 2 can be reduced with NaBH4 in ethanol to form N-(2′,4′,6′-triphenylbenzyl)-2-aminop
