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

501653-22-1

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501653-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501653-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,6,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501653-22:
(8*5)+(7*0)+(6*1)+(5*6)+(4*5)+(3*3)+(2*2)+(1*2)=111
111 % 10 = 1
So 501653-22-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN2O2/c8-4-6-9-7(10-12-6)5-2-1-3-11-5/h1-3H,4H2

501653-22-1SDS

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 5-(chloromethyl)-3-(furan-2-yl)-1,2,4-oxadiazole

1.2 Other means of identification

Product number -
Other names BB_SC-3290

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:501653-22-1 SDS

501653-22-1Downstream Products

501653-22-1Relevant academic research and scientific papers

Design, synthesis and biological evaluation of triaryl compounds as novel 20S proteasome inhibitors

Yang, Yajun,Wang, Ke,Wu, Bo,Yang, Ying,Lai, Fangfang,Chen, Xiaoguang,Xiao, Zhiyan

, (2020/09/02)

Thirty novel triaryl compounds were designed and synthesized based on the known proteasome inhibitor PI-1840. Most of them showed significant inhibition against the β5c subunit of human 20S proteasome, and five of them exhibited IC50 values at the sub-micromolar level, which were comparable to or even more potent than PI-1840. The most active two (1c and 1d) showed IC50 values of 0.12 and 0.18 μM against the β5c subunit, respectively, while they displayed no obvious inhibition against the β2c, β1c and β5i subunits. Molecular docking provided informative clues for the subunit selectivity. The potent and subunit selective proteasome inhibitors identified herein represent new chemical templates for further molecular optimization.

Triaryl compound and preparation method and pharmaceutical application thereof

-

, (2020/12/14)

The invention discloses a triaryl compound as shown in a formula I which is described in the specification, physiologically acceptable salt, a preparation method of the compound, a pharmaceutical preparation containing the compound, and application of the

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