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1H-Tetrazole, 5-(4-chlorophenoxy)-, also known as 4-(5-tetrazolyl)phenoxychloride, is a chemical compound with the molecular formula C7H4ClN4O and a molecular weight of 198.59 g/mol. It is a white to off-white crystalline solid that is soluble in water and various organic solvents. 1H-Tetrazole, 5-(4-chlorophenoxy)- is primarily used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its reactivity and can form various derivatives, making it a valuable building block in organic chemistry. Due to its potential reactivity and the presence of a chlorophenoxy group, it is important to handle 1H-Tetrazole, 5-(4-chlorophenoxy)- with care, following appropriate safety protocols.

4611-43-2

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4611-43-2 Usage

Structure

A tetrazole derivative containing a chlorophenoxy group

Usage

Commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds, including potential drug candidates

Production

Used in the production of dyes, pigments, and other organic compounds

Biological activities and pharmacological properties

Studied for its potential biological activities and pharmacological properties, making it a valuable chemical in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 4611-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,1 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4611-43:
(6*4)+(5*6)+(4*1)+(3*1)+(2*4)+(1*3)=72
72 % 10 = 2
So 4611-43-2 is a valid CAS Registry Number.

4611-43-2Relevant academic research and scientific papers

CoFe2O4 nanoparticles as a magnetically recoverable and reusable catalyst for the synthesis of arylaminotetrazoles and 5-aryloxytetrazoles

Bahari, Siavash,Rezaei, Akbar

, p. 65 - 68 (2014/03/21)

An efficient and direct method is described for the synthesis of 5-arylamino-1H-tetrazoles (Isomer A) or 1-aryl-5-amino-1Htetrazoles (Isomer B) and 5-aryloxytetrazoles from arylcyanamides or cynates with nano CoFe 2O4 as a reusable a

Kinetics and mechanism of izomerization of N-alkoxycarbonyl-5-aroxytetrazoles

Dabbagh,Mansoori

, p. 1771 - 1781 (2007/10/03)

The kinetics and mechanism of the N2-N1-isomerization of 2-methoxycarbonyl-5-(p-X-phenoxy)-tetrazoles (X = H, CH3, NHCOCH3, Cl, Br, NO2) were studied by 1H NMR spectroscopy in a DMSO-d6-CDCl3 mixture (25: 75). The rate of isomerization of the N2-isomer into N1-isomer fit the first-order equation (after three half-conversion periods). The isomerization is accompanied by hydrolysis and decarboxylation. The Hammett plot of In(kXlkH) for the isomerization showed a good correlation with σ- values (p- = 1.33, r = 0.965). A poor correlation with σ values was obtained. The kinetic data, the effect of solvent polarity, the substituent effects, and the results of AM1 quantum-chemical calculations suggest an ionic mechanism of the isomerization in polar solvents and a concerted mechanism in nonpolar solvents.

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