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1,3-bis(4-methyl-1,2,5-oxadiazol-3-yl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

339243-28-6

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339243-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 339243-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,2,4 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 339243-28:
(8*3)+(7*3)+(6*9)+(5*2)+(4*4)+(3*3)+(2*2)+(1*8)=146
146 % 10 = 6
So 339243-28-6 is a valid CAS Registry Number.

339243-28-6SDS

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-bis(4-methyl-1,2,5-oxadiazol-3-yl)urea

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:339243-28-6 SDS

339243-28-6Downstream Products

339243-28-6Relevant academic research and scientific papers

The influence of the substitution pattern on the molecular conformation of ureido-1,2,5-oxadiazoles, related to STAT3 inhibitors: Chemical behavior and structural investigation

Villa, Stefania,Masciocchi, Daniela,Gelain, Arianna,Meneghetti, Fiorella

experimental part, p. 1240 - 1253 (2012/08/28)

Signal transducer and activator of transcription 3 (STAT3) is a protein constitutively activated by aberrant upstream tyrosine kinase activities in a broad spectrum of human solid and blood tumors. Therefore, the availability of drugs affecting STAT3 may have important therapeutic potential for the treatment of cancer. Pursuing our efforts in exploring the influence of the substitution pattern of the ureido 1,2,5-oxadiazole moiety on the molecular conformation, new compounds substituted at positions 3 and 4 on the furazane ring were synthesized. The inhibition properties vs. STAT3 of the novel compounds were evaluated in a dual-luciferase assay, using HCT-116 cells, and the results evidenced a moderate activity only for the compounds endowed with a planar arrangement. Crystallographic studies of the new derivatives were performed in order to evidence the peculiar chemical behavior and to evaluate how structural modulations affected the biological properties. Copyright

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