14665-22-6 Usage
Description
[1,1'-Biphenyl]-2-carboxaldehyde, 2'-(hydroxyMethyl)is a chemical compound characterized by the molecular formula C14H12O2. It features a biphenyl group with a carboxaldehyde and a hydroxyMethyl group attached at distinct positions, making it a versatile building block in organic synthesis.
Uses
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-2-carboxaldehyde, 2'-(hydroxyMethyl)is utilized as an intermediate in the synthesis of biologically active compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, this compound serves as an intermediate for the production of various compounds with pesticidal or herbicidal properties, aiding in the advancement of agricultural solutions.
Used in Dye and Pigment Production:
[1,1'-Biphenyl]-2-carboxaldehyde, 2'-(hydroxyMethyl)is also employed in the creation of dyes and pigments, thanks to its aromatic structure and synthetic potential.
Used in Specialty Chemicals:
[1,1'-Biphenyl]-2-carboxaldehyde, 2'-(hydroxyMethyl)-'s synthetic versatility extends to the production of specialty chemicals, where it is used to develop unique chemical products for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 14665-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,6 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14665-22:
(7*1)+(6*4)+(5*6)+(4*6)+(3*5)+(2*2)+(1*2)=106
106 % 10 = 6
So 14665-22-6 is a valid CAS Registry Number.
14665-22-6Relevant articles and documents
Flow-vacuum pyrolysis of polycyclic compounds. 221 : Pyrolysis of 2,2'-bis(hydroxymethyl)biphenyl
Istrati, Daniela,Marton, George,Drǎghici, Constantin,Grigore, Adriana,Banciu, Mircea D.
, p. 719 - 724 (2007/10/03)
The flow-vacuum pyrolysis of the title diol, between 600°C - 800°C and 1mm Hg in argon atmosphere, was investigated using GC/MS. The main reaction products were: fluorene, 9-methylfluorene, 9-methylenefluorene; 9,10-dihydrophenanthrene; phenanthrene; 9-hydroxy-9,10-dihydroanthracene; 9-fluorenol; 9-fluorenone; 2-methyl-2'-formylbiphenyl (major product; 38% at 850°C); 2-hydroxymethyl-2'-formylbiphenyl and 2,2'-diphendialdehyde. The amount of products resulted from intramolecular cyclization was 52% at 850°C and the ratio between products with five-member and six-member central ring was 39:13 at 850°C. A radical mechanism explaining the formation of the reaction products is suggested and a comparison between pyrolysis of the title diol and of the previously studied 2,2'-bis(bromomethyl)biphenyl is made.
