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4-methylpentane-2,3-dione 3-oxime is an organic compound with the molecular formula C6H11NO2. It is a derivative of 4-methylpentane-2,3-dione, where an oxime group (-NHOH) is attached to the 3-carbon position. 4-methylpentane-2,3-dione 3-oxime is known for its potential use as a synthetic intermediate in the preparation of various pharmaceuticals and agrochemicals. It is characterized by its ability to form a cyclic structure due to the intramolecular hemiacetal formation between the carbonyl group and the oxime hydroxyl group. The compound is typically synthesized through the reaction of 4-methylpentane-2,3-dione with hydroxylamine, and it is an important building block in organic chemistry due to its reactivity and the variety of transformations it can undergo.

5440-21-1

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5440-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5440-21-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5440-21:
(6*5)+(5*4)+(4*4)+(3*0)+(2*2)+(1*1)=71
71 % 10 = 1
So 5440-21-1 is a valid CAS Registry Number.

5440-21-1SDS

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 (3E)-3-hydroxyimino-4-methylpentan-2-one

1.2 Other means of identification

Product number -
Other names 4-Methyl-pentan-2,3-dion-3-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:5440-21-1 SDS

5440-21-1Relevant academic research and scientific papers

A Novel and Efficient Method for the Preparation of α-Hydroxyimino Carbonyl Compounds from α,β-Unsaturated Carbonyl Compounds with Butyl Nitrite and Phenylsilane Catalyzed by a Cobalt(II) Complex

Kato, Koji,Mukaiyama, Teruaki

, p. 2948 - 2953 (2007/10/02)

Various α,β-unsaturated carbonyl compounds, such as α,β-unsaturated esters, α,β-unsaturated ketones, α,β-unsaturated nitriles, and α,β-unsaturated amides, were directly converted to the corresponding α-hydroxyimino carbonyl compounds in high yields on treatment with butyl nitrite and phenylsilane in the presence of a catalytic amount of N,N'-bis(2-ethoxycarbonyl-3-oxobutylidene)ethylenediaminatocobalt(II) complex under mild conditions.

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