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2-(3-chlorophenyl)oxazolo[4,5-b]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52333-56-9

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52333-56-9 Usage

Heterocyclic structure

The compound contains both an oxazole and pyridine ring.

Chemical compound

2-(3-chlorophenyl)oxazolo[4,5-b]pyridine is a chemical compound.

Medicinal chemistry

It is primarily used in the field of medicinal chemistry.

Drug development

The compound is a potential candidate for drug development.

Unique structure and properties

These make it a promising candidate for targeting specific biological pathways or proteins.

Potential applications

The compound may have potential applications in the treatment of various diseases and disorders.

Further research necessary

More research and testing are needed to fully understand its pharmacological potential.

Specific interactions and mechanisms of action

These have yet to be fully elucidated.

Check Digit Verification of cas no

The CAS Registry Mumber 52333-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52333-56:
(7*5)+(6*2)+(5*3)+(4*3)+(3*3)+(2*5)+(1*6)=99
99 % 10 = 9
So 52333-56-9 is a valid CAS Registry Number.

52333-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-chlorophenyl)-[1,3]oxazolo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 2-(3-Chlorophenyl)oxazolo[4,5-b]pyridine

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:52333-56-9 SDS

52333-56-9Downstream Products

52333-56-9Relevant academic research and scientific papers

In vitro and in silico evaluation of 2-(substituted phenyl) oxazolo[4,5-b]pyridine derivatives as potential antibacterial agents

Reen, Gagandeep Kour,Kumar, Ashok,Sharma, Pratibha

, p. 3336 - 3344 (2017/10/06)

Increasing resistance to antibiotics is a major problem worldwide and stimulates the development of new bacterial inhibitors. Series of oxazolo[4,5-b]pyridine synthesized in our lab was examined to screen them as potential antimicrobial agents. The antimi

Acid-Catalyzed, Silica-Supported, One-Pot Benzoylation Route to Synthesize 2-(Substituted Phenyl)oxazolo[4,5-b]pyridines under Ambient Conditions

Reen, Gagandeep Kour,Dudhe, Premansh,Ahuja, Monika,Kumar, Ashok,Sharma, Pratibha

supporting information, p. 1986 - 1994 (2015/08/18)

The present paper describes a silica-supported, perchloric-acid-catalyzed, efficient protocol for the synthesis of 2-(phenyl)oxazolo[4,5-b]pyridine derivatives. This strategy has high conversion, simple workup procedures, ambient conditions, short reactio

A rapid method for the preparation of 2-substituted oxazolo[4,5-b]pyridines using microwave-assisted direct condensation reactions

Myllym?ki, Mikko J.,Koskinen, Ari M.P.

, p. 2295 - 2298 (2007/10/03)

The condensation reaction of 2-amino-3-hydroxypyridine with different carboxylic acids by microwave-assisted heating is a fast method for producing libraries based on fused 2-substituted oxazolo[4,5-b]pyridines in moderate to good yields.

Anti-inflammatory oxazole[4,5-b]pyridines

-

, (2008/06/13)

The various isomers of oxazolo- and thiazolopyridines having utility as antiinflammatory, antipyretic and analgesic agents are prepared by condensation of an appropriate amino-hydroxypyridine or amino-mercaptopyridine with a carboxylic acid, halide or anhydride.

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