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95-34-1

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95-34-1 Usage

Structure

Heterocyclic aromatic compound with two benzoimidazole rings connected by a double bond, resulting in a unique and complex structure

Biological Activities

Anticancer: Potential for cancer treatment
Antiviral: Ability to combat viral infections
Antimicrobial: Efficacy against various microbes

Potential Applications

Medicinal Chemistry: Utilized in pharmaceutical research and drug development
Fluorescent Probe: Investigated for its role in DNA and RNA detection through fluorescence

Research Significance

Further exploration may lead to advancements in medicine and scientific understanding.

Check Digit Verification of cas no

The CAS Registry Mumber 95-34-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95-34:
(4*9)+(3*5)+(2*3)+(1*4)=61
61 % 10 = 1
So 95-34-1 is a valid CAS Registry Number.

95-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(1H-benzoimidazol-2-yl)ethenyl]-1H-benzoimidazole

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:95-34-1 SDS

95-34-1Relevant articles and documents

Thermally Induced trans-to-cis Isomerization and Its Photoinduced Reversal Monitored using Absorption and Luminescence: Cooperative Effect of Metal Coordination and Steric Substituent

Zhang, Jun-Quan,Zhang, De-Shan,Chen, Qiu-Jie,Xu, Hai-Bing,Kurmoo, Mohamedally,Zeng, Ming-Hua

, p. 5177 - 5185 (2019/03/17)

For ethene derivatives with large groups the cis-isomer is often quite unstable and unavailable. Herein, we report an exception of two stable coordination complexes, (cis-L)ZnCl2, starting from trans-1,2-bis(1-R-benzo[d]imidazol-2-yl)ethene (R=H, L1; R=CH3, L2) ligands under solvothermal condition (T ≥140 °C). Using the intensity of the absorption and luminescence spectra as probes we proposed its progressive cis-to-trans reversal upon irradiation with UV light, which was confirmed by powder X-ray diffraction (PXRD). Similar results observed in the series of (cis-L2)MIICl2 [M=Fe (4), Co (5), Ni (6)] demonstrate the universal strategy. The results of PXRD, NMR spectroscopy, ESI-MS and DFT calculations support the above conclusion. NMR spectroscopy indicates that irradiation of 1 converts an optimized 71 % of the cis-isomer to trans, whereas the free trans-L1 ligand transforms to only 15 % cis-isomer under similar conditions.

A Simple Synthesis of 2,2'-Bisbenzimidazolylethylen And Its Analogues

Dash, Bhabagrahi,Dora, Essilidi K.,Panda, Chandra S.

, p. 697 - 698 (2007/10/02)

o-Aminomaleanilic acid (IIa) has been conveniently prepared and employed as a novel synthon for one-step synthesis of 2,2'-bisbenzimidazolylethylene (IIIa) in polyphosphoric acid medium.Analogous compounds (IIIb-f)have also been synthesized from o-hydroxy- and o-mercaptomaleanilic acids (IIb and IIc) following a similar procedure.

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