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4-methylnicotinaldehyde oxime is an organic compound with the chemical formula C7H8N2O. It is derived from 4-methylnicotinaldehyde, a derivative of nicotinaldehyde, by the addition of a hydroxyl group (-OH) to the carbon atom adjacent to the carbonyl group (C=O), forming an oxime. 4-methylnicotinaldehyde oxime is characterized by its aldehyde group, which is part of the pyridine ring structure, and the presence of a methyl group attached to the pyridine ring. 4-methylnicotinaldehyde oxime is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactive functional groups and potential to form complex molecules.

7250-50-2

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7250-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7250-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7250-50:
(6*7)+(5*2)+(4*5)+(3*0)+(2*5)+(1*0)=82
82 % 10 = 2
So 7250-50-2 is a valid CAS Registry Number.

7250-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (NE)-N-[(4-methylpyridin-3-yl)methylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 4-Methyl-3-formyl-pyridin-oxim

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:7250-50-2 SDS

7250-50-2Upstream product

7250-50-2Downstream Products

7250-50-2Relevant academic research and scientific papers

A practical and cost-efficient, one-pot conversion of aldehydes into nitriles mediated by 'activated DMSO'

Augustine, John Kallikat,Bombrun, Agnes,Atta, Rajendra Nath

experimental part, p. 2223 - 2227 (2011/10/31)

Participation of activated DMSO in the one-pot transformation of aldehydes to nitriles has been described by reacting aldehydes with NHHHCl in DMSO in the absence of any added base or catalyst. The method is applicable to access a wide range of aromatic, heterocyclic, and aliphatic nitriles, in which only water is a byproduct. A straightforward and practical procedure is demonstrated on a multigram scale. Georg Thieme Verlag Stuttgart - New York.

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