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459809-27-9

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459809-27-9 Usage

Molecular structure

2-(4-Methoxycarbonylphenyl)-1H-benzimidazole-5-carboxylic acid consists of a benzimidazole ring fused with a phenyl group and a carboxylic acid functional group attached at position 5.

Substituents

A methoxycarbonyl group is present at position 4 of the phenyl ring.

Chemical class

It is a chemical compound with a complex structure.

Biological activities

The benzimidazole core is known for its diverse biological activities, such as antimicrobial, antiviral, and anticancer properties.

Pharmaceutical applications

Due to its benzimidazole core and carboxylic acid group, it has potential pharmaceutical applications.

Drug design and development

The presence of a carboxylic acid group makes it a candidate for drug design and development, as it can be easily modified to enhance its pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 459809-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,8,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 459809-27:
(8*4)+(7*5)+(6*9)+(5*8)+(4*0)+(3*9)+(2*2)+(1*7)=199
199 % 10 = 9
So 459809-27-9 is a valid CAS Registry Number.

459809-27-9SDS

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 2-(4-methoxycarbonylphenyl)-3H-benzimidazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(4-METHOXYCARBONYLPHENYL)-1H-BENZO[D]IMIDAZOLE-5-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:459809-27-9 SDS

459809-27-9Relevant articles and documents

Substituted 2-phenyl-benzimidazole derivatives: novel compounds that suppress key markers of allergy

Richards, Mark L.,Lio, Shirley Cruz,Sinha, Anjana,Banie, Homayon,Thomas, Richard J.,Major, Michael,Tanji, Mark,Sircar, Jagadish C.

, p. 950 - 969 (2007/10/03)

The pharmacotherapy of allergy and asthma has traditionally focused on the effecter molecules of the allergic cascade, while neglecting targets that play an early role in their development. Reasoning that IgE is central to the expansion of atopic diseases, we identified and extended a novel family of 2-(substituted phenyl)-benzimidazole inhibitors of IgE response. Pharmacological activity depends on an intact phenylbenzimidazole-bis-amide backbone, and is optimized by the presence of lipophilic terminal groups composed of either bis cycloalkyl or combinations of aliphatic and halogen-substituted aromatic groups. These compounds also inhibit IL-4 and IL-5 responses in T cells and CD23 expression on B cells, with potencies that parallel their inhibition of IgE. The broad profile of these compounds thus underscores their potential for treating the multifarious pathology of asthma.

Benzimidazole compounds for modulating IgE and inhibiting cellular proliferation

-

, (2008/06/13)

The present invention is directed to small molecule inhibitors of the IgE response to allergens, which are useful in the treatment of allergy and/or asthma or any diseases where IgE is pathogenic. This invention also relates to benzimidazole molecules tha

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