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1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114065-33-7

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114065-33-7 Usage

Chemical Family

Oxadiazoles

Explanation

1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)belongs to the family of oxadiazoles, which are heterocyclic organic compounds containing a five-membered ring with oxygen, nitrogen, and two carbon atoms.

Explanation

The molecular formula of 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)is C15H14N2O, indicating the number of carbon (15), hydrogen (14), nitrogen (2), and oxygen (1) atoms present in the compound.

Explanation

The molecular weight of 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)is 238.29 g/mol, which is the sum of the atomic weights of all the atoms in the molecule.

Explanation

As a member of the oxadiazole family, 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)is a heterocyclic organic compound, meaning it contains a ring structure with both carbon and non-carbon atoms.

Explanation

Due to its diverse and useful properties, 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)is utilized in various fields, including pharmaceuticals, agrochemicals, and materials science.

Explanation

Research has been conducted on the potential biological activities and medicinal properties of 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)and its derivatives, which have demonstrated promise in the treatment of various diseases and conditions.

Explanation

The derivatives of 1,2,4-Oxadiazole, 3-(4-methylphenyl)-5-(phenylmethyl)have shown potential in the treatment of different diseases and conditions, making them an area of interest for further research and development.

Molecular Weight

238.29 g/mol

Heterocyclic Organic Compound

Yes

Applications

Pharmaceuticals, Agrochemicals, and Materials Science

Biological Activities and Medicinal Properties

Studied and Shown Promise

Derivatives

Potential in Disease Treatment

Check Digit Verification of cas no

The CAS Registry Mumber 114065-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114065-33:
(8*1)+(7*1)+(6*4)+(5*0)+(4*6)+(3*5)+(2*3)+(1*3)=87
87 % 10 = 7
So 114065-33-7 is a valid CAS Registry Number.

114065-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzyl-3-(4-methylphenyl)-1,2,4-oxadiazole

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:114065-33-7 SDS

114065-33-7Downstream Products

114065-33-7Relevant academic research and scientific papers

One-pot synthesis of 1,2,4-oxadiazoles from carboxylic acid esters and amidoximes using potassium carbonate

Amarasinghe, Kande K.D.,Maier, Matthew B.,Srivastava, Anil,Gray, Jeffrey L.

, p. 3629 - 3631 (2007/10/03)

A convenient one-pot synthesis of 1,2,4-oxadiazoles is described. The condensation of carboxylic acid esters and amidoximes in the presence of potassium carbonate was employed to synthesize a variety of mono-, bis- and tris-oxadiazoles in moderate to exce

SYNTHESIS AND THERMOLYSIS OF SOME N-HYDROXIMOYL- AND N-HYDRAZONOYLAZOLES

Plenkiewicz, Jan,Zdrojewski, Tadeusz

, p. 675 - 710 (2007/10/02)

The reactions of nitrile oxides or nitrile imines with pyrazole, imidazole, 1,2,3- and 1,2,4-triazole or tetrazole derivatives yield the appropriate N-hydroximoyl- or N-hydrazonoylazoles.Thermolysis of 1-hydroximoyltetrazoles, depending on the nature of the substituents in the tetrazole ring, yields 1,2,4-oxadiazoles or 5-amino-1,2,4-oxadiazoles upon hydrazoic acid or nitrogen evolution.Under similar conditions, 1-hydrazonoyltetrazoles give 1,2,4-triazoles or 5-amino-1,2,4-triazoles while 2-hydrazonoyltetrazoles decompose to the dihydro-1,2,4,5-tetrazine derivatives.

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