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22260-71-5

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22260-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22260-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,6 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22260-71:
(7*2)+(6*2)+(5*2)+(4*6)+(3*0)+(2*7)+(1*1)=75
75 % 10 = 5
So 22260-71-5 is a valid CAS Registry Number.

22260-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxy-2-phenyl-4-(4-pyridyl)oxazole

1.2 Other means of identification

Product number -
Other names 2-phenyl-4-pyridin-4-yl-oxazol-5-ol

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:22260-71-5 SDS

22260-71-5Relevant articles and documents

Identification of a Chromogen in the Assay of Hippuric Acid with Acetic Anhydride, Pyridine, and 4-(Dimethylamino)benzaldehyde

Hirota, Kazuhiro,Ikeda, Mikiko,Kawase, Michi,Ohmori, Shinji

, p. 2087 - 2090 (2007/10/02)

A yellow chromogen, formed in the assay system for hippuric acid which consists of acetic anhydride, pyridine, and 4-(dimethylamino)benzaldehyde, was isolated, and the structure was determined to be 4-(1-acetyl-4(1H)-pyridylidene)-2-phenyl-2-oxazolin-5-one.The structure was confirmed by the chemical conversion to known compounds as well as by NMR spectra.The conversion was accomplished by hydrolysis of the chromogen to 4-((benzoylamino)methyl)pyridine, 4-(aminomethyl)pyridine, and benzoic acid via 5-hydroxy-2-phenyl-4-(4-pyridyl)oxazole. 4-(Dimethylamino)benzaldehyde included in the assay system increased the production of the chromogen.The formation mechanism of the chromogen via an intermediate susceptible to oxidation was proposed.

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