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6-methyl-2-(6-methylpyridin-2-yl)-1H-benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67273-47-6

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67273-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67273-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,7 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67273-47:
(7*6)+(6*7)+(5*2)+(4*7)+(3*3)+(2*4)+(1*7)=146
146 % 10 = 6
So 67273-47-6 is a valid CAS Registry Number.

67273-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-(6-methylpyridin-2-yl)-1H-benzimidazole

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:67273-47-6 SDS

67273-47-6Downstream Products

67273-47-6Relevant academic research and scientific papers

Differential antiproliferative activity of new benzimidazole-4,7-diones

Garuti, Laura,Roberti, Marinella,Pizzirani, Daniela,Pession, Annalisa,Leoncini, Emanuela,Cenci, Valentina,Hrelia, Silvana

, p. 663 - 668 (2007/10/03)

Ten benzimidazole-4,7-diones were synthesized and tested in vitro on two tumor cell lines. Several compounds showed a significant antiproliferative activity on K562 cells, although to a different extent, whereas compound 1i showed a highly significant activity on SW620 cells, comparable to that of doxorubicin. Both the substituents in the quinone ring and the position of the nitrogen atom in the pyridine moiety play a crucial role for the biological activity.

Synthesis and antiinflammatory activity of some 2-(substituted-pyridinyl)benzimidazoles

Tsukamoto,Yoshino,Kohno,Ohtaka,Kagaya,Ito

, p. 734 - 738 (2007/10/02)

A series of 2-(2-pyridinyl)benzimidazoles was synthesized and evaluated for antiinflammatory activity by the carrageenan-induced rat paw edema assay. Among several active derivatives, 2-(5-ethylpyridin-2-yl)benzimidazole was selected for further study. A comparison of this compound with phenylbutazone and tiaramide revealed that it possesses stronger activity in acute inflammatory models possibly with slightly less gastrointestinal irritation than both phenylbutazone and tiaramide.

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