5089-22-5 Usage
Description
Fluorescent Brightener 367 is a bright green crystalline powder that exhibits a bright bluish shade. It has a melting point of 210-212°C, a purity of at least 99%, and a fineness of 300 mesh minimum. The maximum UV absorption of this brightener is at 370 nm.
Uses
Used in Textile Industry:
Fluorescent Brightener 367 is used as a whitening and brightening agent for textiles. It enhances the appearance of fabrics by giving them a brighter and more vivid color.
Used in Paper Industry:
In the paper industry, Fluorescent Brightener 367 is used as a brightening agent to improve the whiteness and brightness of paper products.
Used in Detergent Industry:
Fluorescent Brightener 367 is used in detergents and laundry products to whiten and brighten fabrics during washing.
Used in Plastics Industry:
This brightener is also used in the plastics industry to enhance the color and appearance of plastic materials.
Used in Cosmetics Industry:
Fluorescent Brightener 367 is used in cosmetics to provide a brightening effect and improve the appearance of various cosmetic products.
Flammability and Explosibility
Notclassified
TEST ITEMS
SPECIFICATION
METLING POINT
210-212
°
C
PURITY
99% min
FINENESS
300 mesh min
MAX UV ABSORPTION
370mm
Check Digit Verification of cas no
The CAS Registry Mumber 5089-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5089-22:
(6*5)+(5*0)+(4*8)+(3*9)+(2*2)+(1*2)=95
95 % 10 = 5
So 5089-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H14N2O2/c1-2-8-16-15(7-1)17(23-25-19-9-3-5-11-21(19)27-23)13-14-18(16)24-26-20-10-4-6-12-22(20)28-24/h1-14H
5089-22-5Relevant articles and documents
Palladium-catalyzed coupling of azoles or thiazoles with aryl thioethers via C-H/C-S activation
Zhu, Feng,Wang, Zhong-Xia
supporting information, p. 1601 - 1604 (2015/03/30)
Palladium-catalyzed cross-coupling via the Csp2-S bond activation of aryl thioethers and the C-H bond activation of azoles or thiazoles was carried out. Electron-deficient and -rich aryl methyl thioethers and diaryl thioethers can be employed as the coupling partners and the reaction tolerates a range of functional groups including MeO, CF3, CN, PhCO, CONEt2, and Py groups.
Eine einfache Methode zur Herstellung von Benzoxazolen
Seha, Zdenek,Weis, Claus D
, p. 413 - 419 (2007/10/02)
The preparation of benzoxazoles by a facile one-pot reaction is reported.The reaction of carboxylic acids with 2-chloro-N-methyl-Δ1-pyrrolinium chloride in an excess of N-methyl-2-pyrrolidone afforded carboxylic acid chlorides which were converted subsequently to their 2-hydroxyanilides by addition of 2-aminophenols.Cyclization of the 2-hydroxy-anilides at elevated temperatures furnished the benzoxazoles in high yield and purity.