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N-(1H-benzoimidazol-2-yl)-4-nitro-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36855-68-2

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36855-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36855-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,5 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36855-68:
(7*3)+(6*6)+(5*8)+(4*5)+(3*5)+(2*6)+(1*8)=152
152 % 10 = 2
So 36855-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N4O3/c19-13(9-5-7-10(8-6-9)18(20)21)17-14-15-11-3-1-2-4-12(11)16-14/h1-8H,(H2,15,16,17,19)

36855-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1H-benzimidazol-2-yl)-4-nitrobenzamide

1.2 Other means of identification

Product number -
Other names N-(2-Benzimidazolyl)-4-nitrobenzamid

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:36855-68-2 SDS

36855-68-2Relevant academic research and scientific papers

Discovery and initial SAR of inhibitors of interleukin-1 receptor-associated kinase-4

Powers, Jay P.,Li, Shyun,Jaen, Juan C.,Liu, Jinqian,Walker, Nigel P.C.,Wang, Zhulun,Wesche, Holger

, p. 2842 - 2845 (2007/10/03)

High-throughput screening of a small-molecule compound library resulted in the identification of a novel series of N-acyl 2-aminobenzimidazoles that are potent inhibitors of interleukin-1 receptor-associated kinase-4.

13C NMR spectra and biological activity of N-(1H-benzimidazol-2- yl)benzamides

Pilyugin,Sapozhnikov,Davydov,Chikisheva,Vorob'eva,Klimakova,Kiseleva,Kuznetsova,Davletov,Sapozhnikova,Yumadilov

, p. 1653 - 1659 (2008/02/09)

Derivatives of 1H-benzimidazol-2-amine and halo-, nitro-, methoxy-, and hydroxy-substituted benzoic acids were synthesized, and their fungicide activity against pure Fusarium culmorum and Helminthosporium sativum cultures and pathogenic microflora of wheat and barley seeds in laboratory and field tests was studied. Some compounds were found to exhibit a strong fungicide activity. Nauka/Interperiodica 2006.

Synthesis, crystal structure determination and antiproliferative evaluation of novel benzazoyl benzamides

Starcevic, Kristina,Caleta, Irena,Cincic, Dominik,Kaitner, Branko,Kralj, Marijeta,Ester, Katja,Karminski-Zamola, Grace

, p. 2285 - 2299 (2007/10/03)

A series of benzazoyl-benzamides containing different substituents (7-17) were synthesized by condensation of 2-aminobenzazole derivatives (3a-6) with p-substituted benzoyl chlorides. All compounds were characterized by IR, 1H and 13C NMR, MS and elemental analysis. Crystal structure was determined for the compound (9). Some of the new synthesized compounds (7-17) were screened for antitumor activities. Based on presented in vitro screening results we may conclude that compounds (10, 15a, 15b and 16) showed accentuated cell growth inhibitory activity.

SYNTHESIS OF 4-ARYL BENZIMIDAZOLO-s-TRIAZIN-2-ONES AND 2-AROYLAMINOBENZIMIDAZOLO-1,2,4-THIADIAZOLINES

Sridevi, G.,Rao, P. Jayaprasad,Reddy, K. Kondal

, p. 965 - 972 (2007/10/02)

Reaction of 2-aminobenzimidazole with aroylisothiocyanates gave 2-aroylaminobenzimidazoles (3) and N-aroyl-N'-(benzimidazol-2-yl)-thioureas (4).The products obtained on reaction of 4 with PCl5 in POCl3 , and with oxidising agents have been identified as 4

Tautomerie von Heterocyclen, VIII. N-Acylsubstituierte Chlorformamidine als Heterocyclen- Bausteine

Ried, Walter,Erle, Hanns-Eberhard

, p. 475 - 482 (2007/10/02)

N-(4-Nitrobenzoyl)-1-pyrrolidinecarbimidoyl chloride (1) reacts with bisnucleophilic reagents according to two possible pathways to differently structured heterocyclic compounds.In path A following the substitution of the chlorine atom ring closure from t

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