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Acetaldehyde, (2,4-dichlorophenoxy)-, oxime is a chemical compound with the molecular formula C8H7Cl2NO2. It is an oxime derivative of 2,4-dichlorophenoxy acetaldehyde, which is formed by the reaction of acetaldehyde with hydroxylamine in the presence of a catalyst. Acetaldehyde, (2,4-dichlorophenoxy)-, oxime is an important intermediate in the synthesis of various agrochemicals, particularly herbicides, due to its ability to form esters with carboxylic acids. The oxime group in Acetaldehyde, (2,4-dichlorophenoxy)-, oxime is known for its reactivity and can undergo further chemical transformations, making it a versatile building block in organic synthesis. It is also worth noting that due to the presence of chlorine atoms, Acetaldehyde, (2,4-dichlorophenoxy)-, oxime may have potential environmental and health considerations, which underscores the importance of proper handling and disposal in industrial applications.

2776-05-8

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2776-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2776-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2776-05:
(6*2)+(5*7)+(4*7)+(3*6)+(2*0)+(1*5)=98
98 % 10 = 8
So 2776-05-8 is a valid CAS Registry Number.

2776-05-8SDS

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 N-[2-(2,4-dichlorophenoxy)ethylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 2,4-dichlorophenoxyacetaldoxime

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:2776-05-8 SDS

2776-05-8Relevant academic research and scientific papers

Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles

Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.

, p. 856 - 860 (2007/10/02)

The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.

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