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2622-60-8

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2622-60-8 Usage

Uses

1-phenyl-1h-benzo[d]imidazole is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 2622-60-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2622-60:
(6*2)+(5*6)+(4*2)+(3*2)+(2*6)+(1*0)=68
68 % 10 = 8
So 2622-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2/c1-2-6-11(7-3-1)15-10-14-12-8-4-5-9-13(12)15/h1-10H

2622-60-8SDS

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 1-PHENYL-1H-BENZOIMIDAZOLE

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole, 1-phenyl-

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:2622-60-8 SDS

2622-60-8Relevant articles and documents

Osmium(II)-bis(dihydrogen) complexes containing C aryl, C NHC-chelate ligands: Preparation, bonding situation, and acidity

Bolao, Tamara,Esteruelas, Miguel A.,Fernndez, Israel,Oate, Enrique,Palacios, Adrin,Tsai, Jui-Yi,Xia, Chuanjun

, p. 778 - 789 (2015)

The hexahydride complex OsH6(PiPr3)2 (1) reacts with the BF4-salts of 1-phenyl-3-methyl-1-H-benzimidazolium, 1-phenyl-3-methyl-1-H-5,6-dimethyl-benzimidazolium, and 1-phenyl-3-methyl-1-H-imidazolium t

Heteroleptic platinum(ii) NHC complexes with a ?C? cyclometalated ligand-synthesis, structure and photophysics

Tronnier, Alexander,Heinemeyer, Ute,Metz, Stefan,Wagenblast, Gerhard,Muenster, Ingo,Strassner, Thomas

, p. 1680 - 1693 (2015)

Platinum(ii) complexes [(NHC)Pt(L)] with various β-diketonate based auxiliary ligands (L: 3-meacac = 3-methylacetylacetonato, dpm = dipivaloylmethanato, dbm = dibenzoylmethanato, mesacac = dimesitoylmethanato, duratron = bis(2,3,5,6-tetramethylbenzoyl)methanato) and a ?C? cyclometalated N-heterocyclic carbene ligand (NHC: dpbic = 1,3-diphenylbenzo[d]imidazol-2-ylidene, dpnac = 1,3-diphenylnaphtho[2,3-d]imidazol-2-ylidene or bnbic = 1-phenyl-3-benzylbenzo[d]imidazol-2-ylidene) were found to show different aggregation and photophysical properties depending on the auxiliary ligand. Eight complexes were prepared from a silver(i)-NHC intermediate by transmetalation, cyclometalation and subsequent treatment with potassium-tert-butanolate and β-diketone. They were fully characterized by standard techniques including 195Pt NMR. Five complexes were additionally characterized by 2D NMR spectroscopy (COSY, HSQC, HMBC and NOESY). Solid-state structures of five complexes could be obtained and show the tendency of the square-planar compounds to form pairs with different Pt-Pt distances depending on the bulkiness of the substituents at the auxiliary ligand. The result of the photophysical measurements in amorphous PMMA films reveals quantum yields of up to 85% with an emission maximum in the blue region and comparatively short decay lifetimes (3.6 μs). Density functional theory (DFT/TD-DFT) calculations were performed to elucidate the emission process and revealed a predominant 3ILCT/3MLCT character. Organic light-emitting devices (OLEDs) comprising one of the complexes achieved 12.6% EQE, 11.9 lm W-1 luminous efficacy and 25.2 cd A-1 current efficiency with a blue emission maximum at 300 cd m-2. The influence of an additional hole-transporter in the emissive layer was investigated and found to improve the device lifetime by a factor of seven.

Twist it! the acid-dependent isomerization of homoleptic carbenic iridium(III) complexes

Osiak, Jaroslaw G.,Setzer, Tobias,Jones, Peter G.,Lennartz, Christian,Dreuw, Andreas,Kowalsky, Wolfgang,Johannes, Hans-Hermann

, p. 3295 - 3298 (2017)

The first successful meridional to facial isomerization of homoleptic carbenic iridium(iii) complexes is presented. The Br?nsted-acid-mediated procedure allows the conversion of large amounts of material and additionally provides an in situ purification b

Methanol as the C1source: Redox coupling of nitrobenzenes and alcohols for the synthesis of benzimidazoles

An, Jie,Lai, Zemin,Li, Hengzhao,Peng, Mengqi,Sun, Yanhao,Yan, Zihan,Yang, Ruoyan,Zhang, Yuntong

supporting information, p. 748 - 753 (2022/02/02)

We present an operationally simple redox coupling for the synthesis of N-1 substituted benzimidazoles using feedstock building block 2-nitroaniline derivatives as the precursors and methanol as the C1 source. Higher atom, step, and redox economies and exc

Copper nanoparticle anchored biguanidine-modified Zr-UiO-66 MOFs: a competent heterogeneous and reusable nanocatalyst in Buchwald-Hartwig and Ullmann type coupling reactions

Veisi, Hojat,Neyestani, Narges,Pirhayati, Mozhgan,Ahany Kamangar, Sheida,Lotfi, Shahram,Tamoradi, Taiebeh,Karmakar, Bikash

, p. 22278 - 22286 (2021/07/02)

We have designed a functionalized metal-organic framework (MOF) of UiO topology as a support, with an extremely high surface area, adjustable pore sizes and stable crystalline coordination polymeric structure and implanted copper (Cu) nanoparticles thereon. The core three dimensional Zr-derived MOF (UiO-66-NH2) was modified with a biguanidine moiety following a covalent post-functionalization approach. The morphological and physicochemical features of the material were determined using analytical methods such as FT-IR, SEM, TEM, EDX, atomic mapping, XRD and ICP-OES. The SEM and XRD results justified the unaffected morphology of Zr-MOF after structural modifications. The as-synthesized UiO-66-biguanidine/Cu nanocomposite was catalytically explored in the aryl and heteroaryl Buchwald-Hartwig C-N and Ullmann type C-O cross coupling reactions with excellent yields. A library of biaryl amine and biaryl ethers was synthesized over the catalyst under mild and green conditions. Furthermore, the catalyst was isolated by centrifugation and recycled 11 times with no significant copper leaching or change in its activity.

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