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355023-92-6

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  • 2-Pyridineaceticacid,alpha-(hydroxyimino)-,(alphaZ)-(9CI)

    Cas No: 355023-92-6

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355023-92-6 Usage

General Description

2-Pyridineaceticacid,alpha-(hydroxyimino)-,(alphaZ)-(9CI) is a chemical compound with the molecular formula C7H7NO3. It is also known by its systematic name, (Z)-2-(1-Hydroxyiminoethyl)pyridine-3-carboxylic acid. 2-Pyridineaceticacid,alpha-(hydroxyimino)-,(alphaZ)-(9CI) belongs to the class of organic compounds known as pyridine carboxylic acids. It is a derivative of pyridine with a carboxylic acid group and a hydroxyimino group attached to the alpha carbon. The chemical structure of 2-Pyridineaceticacid,alpha-(hydroxyimino)-,(alphaZ)-(9CI) makes it suitable for use in various chemical reactions and as a building block in organic synthesis. 2-Pyridineaceticacid,alpha-(hydroxyimino)-,(alphaZ)-(9CI) may have potential applications in pharmaceuticals or other industries, but its specific uses and properties would need to be further investigated through research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 355023-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,0,2 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 355023-92:
(8*3)+(7*5)+(6*5)+(5*0)+(4*2)+(3*3)+(2*9)+(1*2)=126
126 % 10 = 6
So 355023-92-6 is a valid CAS Registry Number.

355023-92-6SDS

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 2-Pyridineaceticacid,α-(hydroxyimino)-,(alphaZ)-(9CI)

1.2 Other means of identification

Product number -
Other names -

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

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More Details:355023-92-6 SDS

355023-92-6Upstream product

355023-92-6Downstream Products

355023-92-6Relevant articles and documents

Relative reactivity of anti- and syn-oximino carbonates and carbamates of 2-pyridylacetic acid esters

Kim, Ha Young,Lantrip, Douglas A.,Fuchs, Philip L.

, p. 2137 - 2140 (2007/10/03)

(Matrix presented) anti-Oximes of 2-pyridylacetic acid esters are rapidly transformed to pyridine-2-carbonitrile under a variety of conditions while syn-oximes bearing tert-butyl esters can be conveniently deprotected to the corresponding carboxylic acid with subsequent fragmentation to the nitrile.

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