79881-33-7 Usage
Description
4-(2,6-dichlorophenyl)phenol is a member of the hydroxybiphenyls class, specifically biphenyl-4-ol with chlorine atoms substituted at positions 2 and 6.
Uses
Used in Chemical Synthesis:
4-(2,6-dichlorophenyl)phenol is used as a chemical intermediate for the synthesis of various organic compounds and pharmaceuticals, due to its unique structure and reactivity.
Used in Pesticide Industry:
4-(2,6-dichlorophenol)phenol is used as an active ingredient in some pesticides, for its ability to control pests and protect crops, due to its biocidal properties.
Used in Dyeing and Tanning Industry:
4-(2,6-dichlorophenyl)phenol is used as a dyestuff and tanning agent, for its ability to bind with proteins and impart color, due to its reactive functional groups.
Used in Wood Preservation:
4-(2,6-dichlorophenyl)phenol is used as a wood preservative, for its ability to protect wood from decay and insect damage, due to its biocidal properties.
Used in Research and Development:
4-(2,6-dichlorophenyl)phenol is used as a research compound in various scientific studies, for its potential applications in different fields, due to its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 79881-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,8 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79881-33:
(7*7)+(6*9)+(5*8)+(4*8)+(3*1)+(2*3)+(1*3)=187
187 % 10 = 7
So 79881-33-7 is a valid CAS Registry Number.
79881-33-7Relevant articles and documents
ERbeta ligands. Part 1: the discovery of ERbeta selective ligands which embrace the 4-hydroxy-biphenyl template.
Edsall Jr., Richard J,Harris, Heather A,Manas, Eric S,Mewshaw, Richard E
, p. 3457 - 3474 (2003)
The synthesis and structure-activity relationships of a series of simple biphenyls is described. Optimization of the 4-hydroxy-biphenyl template led to compounds with ERbeta selectivity on the order of 20-70-fold.
