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5089-22-5

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5089-22-5 Usage

Flammability and Explosibility

Notclassified

Properties and Applications

TEST ITEMS SPECIFICATION APPEARANCE BRIGHT GREEN CRYSTALLINE POWDER SHADE BRIGHT BLUISH METLING POINT 210-212 ° C PURITY 99% min FINENESS 300 mesh min MAX UV ABSORPTION 370mm

TEST ITEMS

SPECIFICATION

APPEARANCE

BRIGHT GREEN CRYSTALLINE POWDER

SHADE

BRIGHT BLUISH

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

5089-22-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Bis(2-benzoxazolyl)naphthalene

1.2 Other means of identification

Product number -
Other names Fluorescent Brightener 367

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5089-22-5 SDS

5089-22-5Downstream Products

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.

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