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4-PYRIDYLCARBINOL N-OXIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22346-75-4

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22346-75-4 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 22346-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,4 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22346-75:
(7*2)+(6*2)+(5*3)+(4*4)+(3*6)+(2*7)+(1*5)=94
94 % 10 = 4
So 22346-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c8-5-6-1-3-7(9)4-2-6/h1-4,8H,5H2

22346-75-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (P67609)  4-PyridylcarbinolN-oxide  98%

  • 22346-75-4

  • P67609-1G

  • 599.04CNY

  • Detail

  • Aldrich

  • (P67609)  4-PyridylcarbinolN-oxide  98%

  • 22346-75-4

  • P67609-5G

  • 2,564.64CNY

  • Detail

22346-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-oxidopyridin-1-ium-4-yl)methanol

1.2 Other means of identification

Product number -
Other names 4-pyridylmethanol N-oxide

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:22346-75-4 SDS

22346-75-4Upstream product

22346-75-4Relevant academic research and scientific papers

Oxidation of N-heterocycles by H2O2 catalyzed by a Mn-porphyrin: An easy access to N-oxides under mild conditions

Thellend,Battioni,Sanderson,Mansuy

, p. 1387 - 1388 (2007/10/03)

A variety of N-heteroaromatic compounds were converted into their corresponding N-oxides with good yields and with high chemoselectivity in tile presence of hydrogen peroxide as oxygen donor and a catalytic amount of Mn-porphyrin. The scope and limitation of this method are discussed.

FURTHER FUNCTIONAL GROUP OXIDATIONS USING SODIUM PERBORATE

McKillop, Alexander,Kemp, Duncan

, p. 3299 - 3306 (2007/10/02)

Sodium perborate in acetic acid is an effective reagent for the oxidation of aromatic aldehydes to carboxylic acids, iodoarenes to (diacetoxyiodo)arenes, azines to N-oxides, and various types of sulfur heterocycles to S,S-dioxides.Nitriles are unaffected by the reagent in acetic acid, but undergo smooth hydration to amides when aqueous methanol is employed as solvent.

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