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6602-28-4

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6602-28-4 Usage

Chemical Properties

light yellow to beige fine crystalline powder

Uses

3-Hydroxypyridine N-oxide was used to study the substrate specificity of dimethyl sulfoxide reductase, isolated from anaerobically grown Escherichia coli.

General Description

3-Hydroxypyridine N-oxide exists in ethanol in the form of free base and in acid medium in the form of conjugate acid.

Check Digit Verification of cas no

The CAS Registry Mumber 6602-28-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6602-28:
(6*6)+(5*6)+(4*0)+(3*2)+(2*2)+(1*8)=84
84 % 10 = 4
So 6602-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NO2/c7-5-2-1-3-6(8)4-5/h1-4,7H

6602-28-4 Well-known Company Product Price

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  • Aldrich

  • (122521)  3-HydroxypyridineN-oxide  99%

  • 6602-28-4

  • 122521-5G

  • 370.89CNY

  • Detail

6602-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Pyridinol N-oxide

1.2 Other means of identification

Product number -
Other names 1-oxidopyridin-1-ium-3-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:6602-28-4 SDS

6602-28-4Relevant articles and documents

Method for synthesizing 3-hydroxy-2-picolinic acid and derivatives thereof

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Paragraph 0044-0045, (2020/12/31)

The invention discloses an effective synthesis method of 3-hydroxy-2-picolinic acid and derivatives thereof. The method comprises an oxidation reaction, a cyanation reaction and a hydrolysis reaction.According to the oxidation reaction, 3-hydroxypyridine as shown in a formula I and derivatives thereof are used as substrates, and under the condition that an aqueous hydrogen peroxide solution is used as an oxidizing agent, the reaction is performed in glacial acetic acid at 60 DEG C in a nitrogen environment to obtain an oxidation product as shown in a structural general formula II. According to the cyanation reaction, the compound II and trimethylsilyl cyanide are taken as substrates and mixed with dimethylaminoformyl chloride in an ice bath, and then the reaction is conducted in dichloromethane at room temperature in the nitrogen environment to obtain a cyanation product as shown in a structural general formula III. According to the hydrolysis reaction, with the product as shown in the formula III as a substrate, the reaction is conducted in ethanol at a temperature of 80 DEG C under the condition of an aqueous sodium hydroxide solution to obtain the 3-hydroxy-2-picolinic acid asshown in the structural general formula IV and the derivatives thereof. The method is relatively economical, reaction universality is good, gram-level preparation is easy to carry out, the whole process can be industrialized, and reaction conditions are green.

Grafting of a rhenium-oxo complex on Schiff base functionalized graphene oxide: An efficient catalyst for the oxidation of amines

Khatri, Praveen K.,Choudhary, Shivani,Singh, Raghuvir,Jain, Suman L.,Khatri, Om P.

, p. 8054 - 8061 (2014/05/20)

A rhenium-oxo complex such as methyltrioxorhenium (MTO) has been homogeneously immobilized on a Schiff base modified graphene oxide (GrO) support via covalent bonding. The loading of MTO on GrO nanosheets was monitored by FTIR, TG-DTA, and elemental analyses. The developed heterogeneous catalyst is found to be efficient for the oxidation of various amines to the corresponding N-oxides using hydrogen peroxide as an oxidant in high to excellent yields. At the end of the reaction, the catalyst is readily recovered by filtration and reused for subsequent runs. After the third run, the catalyst showed a marginal decrease in catalytic activity owing to the leaching of the MTO complex from the support. This journal is the Partner Organisations 2014.

TRANSFORMATION OF 3-HYDROXYPYRIDINE BY PSEUDOMONAS FLUORESCENS AND RHODOCOCCUS OPACUS STRAINS

Zefirov, N. S.,Modyanova, L. V.,Ouyuntsetseg, A.,Piskunkova, N. F.,Terent'ev, P. B.,et al.

, p. 730 - 731 (2007/10/02)

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