204583-39-1

Basic information

• Product Name: 2-[4,6-Bis([1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-yl]-5-[(2-ethylhexyl)oxy]phenol
• Synonyms: 2-[4,6-Bis([1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-yl]-5-[(2-ethylhexyl)oxy]phenol
• CAS NO: 204583-39-1
• Molecular Formula: C₄₁H₃₉N₃O₂
• Molecular Weight: 605.77
• EINECS: 440-520-9
• Mol File: 204583-39-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 794.525°C at 760 mmHg
• Flash Point: 434.313°C
• Appearance: /
• Density: 1.135g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.607
• PKA: 8.36±0.40(Predicted)
• CAS DataBase Reference: 2-[4,6-Bis([1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-yl]-5-[(2-ethylhexyl)oxy]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4,6-Bis([1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-yl]-5-[(2-ethylhexyl)oxy]phenol(204583-39-1)
• EPA Substance Registry System: 2-[4,6-Bis([1,1'-biphenyl]-4-yl)-1,3,5-triazin-2-yl]-5-[(2-ethylhexyl)oxy]phenol(204583-39-1)

Safety Data

• Hazardous Substances Data: 204583-39-1(Hazardous Substances Data)

Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C41H39N3O2/c1-3-5-12-29(4-2)28-46-36-25-26-37(38(45)27-36)41-43-39(34-21-17-32(18-22-34)30-13-8-6-9-14-30)42-40(44-41)35-23-19-33(20-24-35)31-15-10-7-11-16-31/h6-11,13-27,29,45H,3-5,12,28H2,1-2H3

Upstream product

• 123-04-6 3-(chloromethyl)heptane 
• 18908-66-2 3-bromomethylheptane 

Relevant articles and documents

Synthesis method of ultraviolet light absorber UV-1600

The invention discloses a synthesis method of an ultraviolet light absorber UV-1600. The method is composed of four steps of reactions: using 4-cyanobiphenyl and urea as raw materials, and carrying out cyclization reaction in the presence of a basic catalyst to obtain 2, 4-bis([1, 1'-biphenyl]-4-yl)-6-hydroxyl-1, 3, 5-triazine, then carrying out chlorination reaction under the action of a chlorination reagent to obtain an intermediate 2, 4-bis([1, 1'-biphenyl]-4-yl)-6-chloro-1, 3, 5-triazine, carrying out alkylation reaction on the intermediate and resorcinol, and then carrying out etherification reaction on the intermediate and halogenated isooctane to obtain UV-1600. The UV-1600 has an important application prospect in the field of ultraviolet light stabilizers due to the good performance of the UV-1600.