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1,2,4-Oxadiazole, 3-methyl-5-[[4-(methylsulfonyl)phenyl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

346629-84-3

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346629-84-3 Usage

Type of compound

Heterocyclic compound

Structure

Contains an oxadiazole ring and a methylsulfonylphenyl group

Potential applications

a. Medicinal chemistry
b. Building block in the synthesis of pharmaceutical drugs and agrochemicals
c. Development of new materials
d. Fluorescent probe for detecting metal ions

Biological activities

a. Anticancer
b. Antimicrobial
c. Anti-inflammatory

Versatility

Diverse potential applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 346629-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,6,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 346629-84:
(8*3)+(7*4)+(6*6)+(5*6)+(4*2)+(3*9)+(2*8)+(1*4)=173
173 % 10 = 3
So 346629-84-3 is a valid CAS Registry Number.

346629-84-3SDS

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 3-methyl-5-[(4-methylsulfonylphenyl)methyl]-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:346629-84-3 SDS

346629-84-3Relevant academic research and scientific papers

Process development and large-scale synthesis of a PDE4 inhibitor

Conlon, David A.,Drahus-Paone, Antoinette,Ho, Guo-Jie,Pipik, Brenda,Helmy, Roy,McNamara, James M.,Shi, Yao-Jun,Williams, J. Michael,Macdonald, Dwight,Deschenes, Denis,Gallant, Michel,Mastracchio, Anthony,Roy, Bruno,Scheigetz, John

, p. 36 - 45 (2012/12/21)

An efficient, scalable synthesis of the PDE4 inhibitor, 6-[1-methyl-1-(methylsulfonyl)ethyl]-8-(3-{(E)-2-(3-methyl-1,2,4-oxadiazol-5-yl) -2-[4-(methylsulfonyl)phenyl]vinyl}phenyl)-quinoline benzenesulfonate (10) is described. The synthesis is highly conve

Discovery of a substituted 8-arylquinoline series of PDE4 inhibitors: Structure-activity relationship, optimization, and identification of a highly potent, well tolerated, PDE4 inhibitor

Macdonald, Dwight,Mastracchio, Anthony,Perrier, Helene,Dube, Daniel,Gallant, Michel,Lacombe, Patrick,Deschenes, Denis,Roy, Bruno,Scheigetz, John,Bateman, Kevin,Li, Chun,Trimble, Laird A.,Day, Stephen,Chauret, Nathalie,Nicoll-Griffith, Deborah A.,Silva, Jose M.,Huang, Zheng,Laliberte, France,Liu, Susana,Ethier, Diane,Pon, Doug,Muise, Eric,Boulet, Louise,Chi, Chung Chan,Styhler, Angela,Charleson, Stella,Mancini, Joseph,Masson, Paul,Claveau, David,Nicholson, Donald,Turner, Mervyn,Young, Robert N.,Girard, Yves

, p. 5241 - 5246 (2007/10/03)

The discovery and SAR of a new series of substituted 8-arylquinoline PDE4 inhibitors are herein described. This work has led to the identification of several compounds with excellent in vitro and in vivo profiles, including a good therapeutic window of em

A preferred synthesis of 1,2,4-oxadiazoles

Pipik, Brenda,Ho, Guo-Jie,Williams, J. Michael,Conlon, David A.

, p. 1863 - 1870 (2007/10/03)

An efficient and high-yielding one-pot synthesis of 1,2,4-oxadiazoles from carboxylic acids and amidoximes is described. Activation of the carboxylic acid using hydroxybenzotriazole (HOBt) and EDC/HCl followed by reaction with an amidoxime generates an oxime ester. Without isolation, the oxime ester is dehydrated to give the oxadiazole ring.

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