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Phenol, 4,4'-[5,5'-bi-1H-benzimidazole]-2,2'-diylbis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137961-52-5

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137961-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137961-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,6 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137961-52:
(8*1)+(7*3)+(6*7)+(5*9)+(4*6)+(3*1)+(2*5)+(1*2)=155
155 % 10 = 5
So 137961-52-5 is a valid CAS Registry Number.

137961-52-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[5-[2-(4-oxocyclohexa-2,5-dien-1-ylidene)-1,3-dihydrobenzimidazol-5-yl]-1,3-dihydrobenzimidazol-2-ylidene]cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4,4'-(1H,1'H-5,5'-bibenzo[d]imidazole-2,2'-diyl)diphenol

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:137961-52-5 SDS

137961-52-5Downstream Products

137961-52-5Relevant academic research and scientific papers

Strong, specific, reversible binding ligands for transfer RNA: Comparison by fluorescence and NMR spectroscopies with distamycin binding for a new structural class of ligand

Bichenkova, Elena V.,Sadat-Ebrahimi, Seyed E.,Wilton, Amanda N.,O'Toole, Niamh,Marks, Debora S.,Douglas, Kenneth T.

, p. 1651 - 1665 (1998)

Binding data are presented for the interaction with brewer's yeast tRNA(Phe) of a new structural family of ligands, symmetrical bis- benzimidazoles. In addition specific perturbations in chemical shifts were detected by 1-dimensional NMR spectroscopy at 400 MHz for some imino and aromatic methyl protons of tRNA(Phe) when the tRNA was titrated with distamycin. Competitive displacement of the benzimidazole by added distamycin was followed fluorescence spectroscopy.

BIS-BENZIMIDAZOLE COMPOUNDS AND METHODS OF USING SAME

-

Paragraph 00558-00560, (2019/06/05)

Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1 ), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.

ANTIBACTERIAL COMPOUNDS

-

Page/Page column 49, (2010/06/20)

Disclosed are compounds of formula (I), which are of use in the treatment of bacterial diseases and infections, to compositions containing those compounds and to methods of treating bacterial diseases and infections using the compounds. In particular, the compounds are useful for the treatment of infection with, and diseases caused by, Clostridium difficile.

New mustard-linked 2-aryl-bis-benzimidazoles with anti-proliferative activity

Le Sann, Christine,Baron, Anne,Mann, John,Van Den Berg, Hendrik,Gunaratnam, Mekala,Neidle, Stephen

, p. 1305 - 1312 (2007/10/03)

We describe new methodology for the synthesis of symmetric bis-benzimidazoles carrying 2-aryl moieties, including 2-[4-(3′- aminopropoxy)phenyl] and 2-[4-(3′-aminopropanamido)phenyl] substituents, together with the synthesis of novel hybrid molecules comprising bis-benzimidazoles in ester and amide combination with the N-mustard chlorambucil. The in vitro activities of these compounds against five cancer cell lines are also provided. The Royal Society of Chemistry 2006.

New developments in thermally stable polymers

Hergenrother, Paul M.

, p. 481 - 491 (2007/10/02)

Advances in high-temperature polymers since 1985 are discussed with the emphasis on the chemistry.High-temperature polymers refer to materials that exhibit glass-transition temperatures > 200 deg C and have the chemical structure expected to provide high thermooxidative stability.Specific polymers or series of polymers were selected to show how the chemical structure influences certain properties.Poly(arylene ethers) and polyimides are the two principal families of polymers discussed.Recent work on poly(arylene ethers) has concentrated on incorporating heterocyclic units within the polymer backbone.Recent polyimide work has centered on the synthesis of new polymers from novel monomers, several containing the trifluoromethyl group strategically located on the molecule.Various members in each of these polymer families display a unique combination of properties, heretofore unattainable.Other families of polymers are also briefly discussed with a polymer from an AB maleimidobenzocyclobutene exhibiting an especially attractive combination of properties.

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