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1H-Imidazole, 4,5-diphenyl-2-(phenylazo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34938-51-7

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34938-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34938-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,3 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34938-51:
(7*3)+(6*4)+(5*9)+(4*3)+(3*8)+(2*5)+(1*1)=137
137 % 10 = 7
So 34938-51-7 is a valid CAS Registry Number.

34938-51-7SDS

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 N-[(4,5-diphenylimidazol-2-ylidene)amino]aniline

1.2 Other means of identification

Product number -
Other names 2-Phenylazo-4,5-diphenyl-imidazol

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:34938-51-7 SDS

34938-51-7Relevant academic research and scientific papers

Synthesis and Chemical Transformations of 1,3-Diaryltetrazolium Salts. Preparation of Mercury(II) and Palladium(II) Complexes of 1,3-Diaryltetrazolylene and Reactions of 5-Substituted 1,3-Diphenyltetrazolium Salts with Nucleophiles

Araki, Shuki,Wanibe, Yasumi,Uno, Fujio,Morikawa, Akinao,Yamamoto, Kaori,et al.

, p. 1149 - 1156 (2007/10/02)

1,3-Diaryltetrazolium salts 5 and 6 have been prepared by nitric acid oxidation of the corresponding 5-thiolates 4.The reaction of 5 with mercury(II) acetate gives (1,3-diaryltetrazolylene)mercury(II) complexes 7, which provide 5-halotetrazolium salts 8-10 by treatment with halogen. 1,3-Diphenyltetrazolylene (16), generated in situ by proton abstraction of 1,3-diphenyltetrazolium salts 5a or 6a, has been trapped with p-(dimethylamino)benzenediazonium tetrafluoroborate to form 18/18'.The palladium(II) complex 19 of 1,3-diphenyltetrazolylene has been prepared by oxidative addition of tetrakis(triphenylphosphane)palladium(0) to 5-chlorotetrazolium salt 8.The reactivity of various 5-substituted tetrazolium salts toward carbon nucleophiles depends on the nature of the substituents at C-5.With electronegative substituents, nucleophilic substitution proceeds at C-5, whereas electron-donating substituents direct the nucleophiles towards N-2 yielding ring-cleaved products.Key Words: Mesoionic compounds / Tetrazolium salts, 1,3-diaryl / Carbenes, mesoionic / Carbene-metal complexes / Nucleophilic substitution

COORDINATION COMPOUNDS OF HETEROCYCLIC AND DERIVATIVES. I-SYNTHESIS AZO CHARACTERIZATION OF BIVALENT METAL CHELATES WITH SOME IMIDAZOLE AZO DYES

Mahmoud, M. R.,El-Hamide, R. Abd,Wahab, A. A. Abdel,Salman, H. M.

, p. 11 - 18 (2007/10/02)

2-(4-R-Phenylazo)-4,5-diphenylimidazole (R = H, PAI; = OH, HPAI; = COOH, CPAI) acts as a bidentate chelating ligand to form stable complexes with Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II) ions.It is concluded that the ligands are bonded to the metal ion through the α-nitrogen atom of the aryl azo group and N-3 of the imidazole ring.The apparent formation constants of the complexes in solution have been determined.

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