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1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI), with the molecular formula C9H8N2, is a heterocyclic organic compound belonging to the imidazopyridine class. It is recognized for its wide-ranging applications, especially in medicinal chemistry where it serves as a key building block for the synthesis of pharmaceutical drugs. Additionally, it is utilized in the development of agrochemicals, dyes, and pigments. 1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) has also garnered interest for its potential biological activities, such as antimicrobial, antiviral, and antitumor properties, making it a multifaceted chemical with significant implications in various scientific and technological domains.

273756-99-3

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273756-99-3 Usage

Uses

Used in Pharmaceutical Industry:
1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical drugs. Its unique structure and properties make it a valuable component in the development of new medications with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) is employed as a building block in the creation of agrochemicals. Its incorporation aids in the development of products designed to protect crops and enhance agricultural productivity.
Used in Dye and Pigment Production:
1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) is utilized in the production of dyes and pigments due to its chemical properties that contribute to color intensity and stability. This makes it a valuable component in industries that rely on colorants for their products.
Used in Antimicrobial Applications:
1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) is studied for its antimicrobial properties, making it a potential candidate for use in applications that require the inhibition of microbial growth, such as in the development of antibiotics or antimicrobial agents for various industries.
Used in Antiviral Applications:
1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI) is explored for its antiviral capabilities, suggesting its potential use in the development of antiviral medications or treatments to combat viral infections.
Used in Antitumor Applications:
1H-Imidazo[4,5-b]pyridine,1-ethyl-(9CI)'s antitumor properties are of interest for its potential use in oncology, where it could be employed in the development of drugs aimed at treating various types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 273756-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,7,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 273756-99:
(8*2)+(7*7)+(6*3)+(5*7)+(4*5)+(3*6)+(2*9)+(1*9)=183
183 % 10 = 3
So 273756-99-3 is a valid CAS Registry Number.

273756-99-3SDS

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 1-ethyl-1H-imidazo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 1-ethyl-4-azabenzimidazole

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:273756-99-3 SDS

273756-99-3Downstream Products

273756-99-3Relevant academic research and scientific papers

S-3578, A new broad spectrum parenteral cephalosporin exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa synthesis and structure-activity relationships

Yoshizawa, Hidenori,Itani, Hikaru,Ishikura, Koji,Irie, Tadashi,Yokoo, Katsuki,Kubota, Tadatoshi,Minami, Kyoji,Iwaki, Tsutomu,Miwa, Hideaki,Nishitani, Yasuhiro

, p. 975 - 992 (2007/10/03)

A series of 7-aminothiadiazolylcephalosporins having a 1-(substituted)-1H-imidazo[4,5-b]pyridinium group at the C-3′ position of the cephem nucleus were synthesized and evaluated for in vitro antibacterial activities. Among the cephalosporins prepared in

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