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1-(3-chlorophenyl)-3-hydroxy-1,2,4-1H-triazole is an organic compound with the chemical formula C7H5ClN2O. It is a derivative of 1,2,4-triazole, featuring a 3-chlorophenyl group attached to the 1-position and a hydroxyl group at the 3-position. 1-(3-chlorophenyl)-3-hydroxy-1,2,4-1H-triazole is known for its potential applications in various chemical and pharmaceutical industries, such as a building block for the synthesis of more complex molecules or as an intermediate in the production of agrochemicals. Due to its reactivity and functional groups, it is important to handle 1-(3-chlorophenyl)-3-hydroxy-1,2,4-1H-triazole with care, following proper safety protocols.

84456-06-4

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84456-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84456-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,5 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84456-06:
(7*8)+(6*4)+(5*4)+(4*5)+(3*6)+(2*0)+(1*6)=144
144 % 10 = 4
So 84456-06-4 is a valid CAS Registry Number.

84456-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-3-hydroxy-1,2,4-1H-triazole

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:84456-06-4 SDS

84456-06-4Relevant academic research and scientific papers

Synthesis of Ethyl 2-propionates and Related Derivatives

Beck, James R.,Babbitt, George E.,Lynch, Michael P.

, p. 1467 - 1470 (2007/10/02)

Alkylation of 1-aryl-1H-1,2,4-triazol-3-ols with ethyl 2-bromopropionate under basic conditions resulted in the formation of 2-propionic acid, ethyl esters.No N-alkylated products were detected.Similar alkylation of 2-oxo-5-phenyl-1,3,4-thiazole and the corresponding 1,3,4-oxadiazole gave only N-alkylated derivatives.With 4-hydroxy-6-phenylpyrimidine and 2-oxo-4-phenylthiazole, both O- and N-alkylation occurred.Structure assignments were based on ir and 13C nmr spectral data.

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