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21645-25-0

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21645-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21645-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,4 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21645-25:
(7*2)+(6*1)+(5*6)+(4*4)+(3*5)+(2*2)+(1*5)=90
90 % 10 = 0
So 21645-25-0 is a valid CAS Registry Number.

21645-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2'-tetrahydropyranoxy)phenol

1.2 Other means of identification

Product number -
Other names 2-Tetrahydropyran-2-yloxy-phenol

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:21645-25-0 SDS

21645-25-0Relevant articles and documents

Design, synthesis and biological evaluation of 2-substituted-6-[(4-substituted-1-piperidyl)methyl]-1H-benzimidazoles as inhibitors of ebola virus infection

Bessières, Maxime,Plebanek, El?bieta,Chatterjee, Payel,Shrivastava-Ranjan, Punya,Flint, Mike,Spiropoulou, Christina F.,Warszycki, Dawid,Bojarski, Andrzej J.,Roy, Vincent,Agrofoglio, Luigi A.

, (2021/02/06)

Novel 2-substituted-6-[(4-substituted-1-piperidyl)methyl]-1H-benzimidazoles were designed and synthesized as Ebola virus inhibitors. The proposed structures of the new prepared benzimidazole-piperidine hybrids were confirmed based on their spectral data and CHN analyses. The target compounds were screened in vitro for their anti-Ebola activity. Among tested molecules, compounds 26a (EC50=0.93 μM, SI = 10) and 25a (EC50=0.64 μM, SI = 20) were as potent as and more selective than Toremifene reference drug (EC50 = 0.38 μM, SI = 7) against cell line. Data suggests that the mechanism by which 25a and 26a block EBOV infection is through the inhibition of viral entry at the level of NPC1. Furthermore, a docking study revealed that several of the NPC1 amino acids that participate in binding to GP are involved in the binding of the most active compounds 25a and 26a. Finally, in silico ADME prediction indicates that 26a is an idealy drug-like candidate. Our results could enable the development of small molecule drug capable of inhibiting Ebola virus, especially at the viral entry step.

Highly efficient synthesis of tetra benzo spiro bis-crown ether

Moradgholi, Fatemeh,Vahedi, Hooshang,Lari, Jalil

, p. 85 - 90 (2015/06/23)

Novel spiro bis-crown ethers derivatives with four benzo units connected via one carbon bridges have been prepared. These compounds represent well preorganized cavities with interesting complexation abilities towards cations. These macrocyclic were prepared by a four-step via template method by utilizing simple precursors catechol, oliethylen glycol and penta erythritol tetra bromide in good yield. Additionally, cesium carbonate could be used as an excellent base for these reactions.

Tuning the mesomorphic properties of liquid-crystalline dibenzotetraaza[14]annulenes - Discotic nematic phases of tetraalkoxy- substituted derivatives

Grolik, Jaros?aw,Dudek, ?ukasz,Eilmes, Julita

scheme or table, p. 5127 - 5130 (2012/09/25)

A homologous series of five tetrasubstituted dibenzotetraaza[14]annulene- based discotic mesogens was prepared and studied using polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). A nematic phase was identified for the product bearing two peripheral isobutoxy and two dodecyloxy substituents.

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