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2-(4-TERT-BUTYLPHENYL)-5-(CHLOROMETHYL)-1,3,4-OXADIAZOLE is a heterocyclic chemical compound with the molecular formula C14H15ClN2O. It features an oxadiazole ring, a tert-butylphenyl group, and a chloromethyl group. 2-(4-TERT-BUTYLPHENYL)-5-(CHLOROMETHYL)-1,3,4-OXADIAZOLE has been studied for its potential applications in pharmaceuticals, pesticides, and materials science due to its unique chemical structure and biological activity.

754214-36-3

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754214-36-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-TERT-BUTYLPHENYL)-5-(CHLOROMETHYL)-1,3,4-OXADIAZOLE is used as a potential drug candidate for the treatment of various diseases. Its unique chemical structure allows it to be a valuable building block for the synthesis of other organic compounds with potential therapeutic applications.
Used in Pesticide Industry:
2-(4-TERT-BUTYLPHENYL)-5-(CHLOROMETHYL)-1,3,4-OXADIAZOLE is used for its antimicrobial and insecticidal properties. It has been investigated for its potential to control pests and protect crops, making it a promising candidate for the development of new pesticides.
Used in Materials Science:
2-(4-TERT-BUTYLPHENYL)-5-(CHLOROMETHYL)-1,3,4-OXADIAZOLE is used as a valuable building block for the synthesis of other organic compounds with potential applications in materials science. Its unique chemical structure can contribute to the development of new materials with specific properties for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 754214-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,4,2,1 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 754214-36:
(8*7)+(7*5)+(6*4)+(5*2)+(4*1)+(3*4)+(2*3)+(1*6)=153
153 % 10 = 3
So 754214-36-3 is a valid CAS Registry Number.

754214-36-3SDS

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 2-(4-tert-butylphenyl)-5-(chloromethyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names butylphenylchloromethyloxadiazole

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:754214-36-3 SDS

754214-36-3Downstream Products

754214-36-3Relevant academic research and scientific papers

Synthesis and antimicrobial properties of 1,3,4-oxadiazole analogs containing dibenzosuberane moiety

Moger, Manjunath,Satam, Vijay,Govindaraju, Darshan Raj C.,Paniraj,Gopinath, Vadiraj S.,Hindupur, Rama Mohan,Pati, Hari N.

, p. 104 - 111 (2014/02/14)

A series of ten novel 1,3,4-oxadiazole analogs containing dibenzosuberane moiety were synthesized using linear as well as convergent synthesis approach. All the compounds were characterized by mass spectrometry, infrared (IR), 1H and 13C nuclear magnetic resonance (1H NMR and 13C NMR) spectroscopies and elemental analysis. These compounds were evaluated for antibacterial and antifungal activities. Among ten analogs, four compounds, namely, 8a, 8d, 8e and 8j were found to be highly active antibacterial and antifungal agents.

Anthracene-tethered aminomethyl oxadiazole chemosensor: A probe offering selective chromo- and fluorogenic signalings for targeting Cu(II)

Mashraqui, Sabir H.,Khan, Tabrez,Chandiramani, Mukesh,Betkar, Rupesh,Poonia, Kiran

experimental part, p. 361 - 367 (2011/11/29)

A new optical chemosensor featuring anthracene as a fluorophore and an aminomethyl oxadiazole moiety as a bidentate chelate has been synthesized. From photophysical studies, we find the probe to offer remarkably selective chromo- and fluorogenic signaling

Microwave-assisted one-step synthesis of substituted 2-chloromethyl-1,3,4- oxadiazoles

Natero, Reina,Koltun, Dmitry O.,Zablocki, Jeffery A.

, p. 2523 - 2529 (2007/10/03)

We have developed a simple one-step synthesis of 2-chloromethyl-1,3,4- oxadiazoles from commercially available acylhydrazides using 1-chloro-2,2,2-trimethoxyethane as a solvent under microwave irradiation.

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