Welcome to LookChem.com Sign In|Join Free

CAS

  • or

124340-93-8

Post Buying Request

124340-93-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

124340-93-8 Usage

General Description

2-Pyridin-4-yl-3H-benzoimidazole-4-carboxylic acid, also known as compound 1, is a synthetic chemical compound with potential anti-cancer properties. It belongs to the class of benzoimidazoles and has a chemical structure comprising a pyridine ring and a benzoimidazole ring. Research has indicated that this compound has the ability to inhibit the growth of cancer cells and induce apoptosis, making it a potential candidate for the development of anti-cancer drugs. Its mechanism of action involves targeting specific cellular pathways involved in cancer cell proliferation, making it a promising compound for further research and drug development in the treatment of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 124340-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124340-93:
(8*1)+(7*2)+(6*4)+(5*3)+(4*4)+(3*0)+(2*9)+(1*3)=98
98 % 10 = 8
So 124340-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3O2/c17-13(18)9-2-1-3-10-11(9)16-12(15-10)8-4-6-14-7-5-8/h1-7H,(H,15,16)(H,17,18)

124340-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyridin-4-yl-1H-benzimidazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(pyridin-4-yl)-1H-benzimidazole-4-carboxylic acid

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:124340-93-8 SDS

124340-93-8Relevant articles and documents

Synthesis and biological evaluation of novel benzimidazole derivatives bearing a heterocyclic ring at 4/5 position

Wubulikasimu, Reyila,Yang, Yanbing,Xue, Fei,Luo, Xianjin,Shao, Dongping,Li, Yuhuan,Gao, Rongmei,Ye, Weidong

, p. 2297 - 2304 (2013/09/24)

A series of novel benzimidazole derivatives bearing a heterocyclic ring as oxadiazole (21-32), thiadiazole (33-34), triazole (35-36) were synthesized and evaluated for their activities against Coxsackie virus B3 and B6 in Vero cells. Compounds 21-26, 31-36 with moieties of 2'-pyridyl, 3'-pyridyl and 4'-pyridyl at the 2-position and oxadiazoles, thiadiazole, or triazole substituent at the 4- or 5-position generally displayed activities against CVB3 and CVB6. Especially compound 24 (IC50 = 1.08 μg/mL, SI = 61.7 against CVB3) was the promising candidate as lead compound for anti-enteroviral drug. It was observed in the incorporation of heterocyclic rings in benzimidazole at the 5-position could enhance their biological activities.

Synthesis and antiviral activity against Coxsackie virus B3 of some novel benzimidazole derivatives

Cheng, Jun,Xie, Jiangtao,Luo, Xianjin

, p. 267 - 269 (2007/10/03)

Some benzimidazole derivatives were synthesized and the antiviral evaluation against Coxsackie virus B3 is reported. These compounds are proved to be excellent inhibitors of CVB3. Some benzimidazole derivatives were synthesized and evaluated for their antiviral properties. Compounds 20 and 21 showed potent selective activity against Coxsackie virus B3 in VERO cells. Some structure-activity relationships were discussed.

Substituted benzimidazoles

-

, (2008/06/13)

Compounds of formula I are suitable for the production of pharmaceuticals for the prophylaxis and therapy of disorders in whose course an increased activity of NFκB is involved.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 124340-93-8