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4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol, also known as CL-316243, is a chemical compound that functions as a selective beta-3 adrenergic receptor agonist. It is widely utilized in laboratory research for its potential to stimulate the breakdown of stored fat in adipose tissue by activating beta-3 adrenergic receptors. 4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol also exhibits promise in the management of metabolic disorders due to its effects on glucose and lipid metabolism.

54221-73-7

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54221-73-7 Usage

Uses

Used in Pharmaceutical Research and Development:
4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol is used as a research tool for the development of new drugs targeting obesity and metabolic disorders. Its agonistic action on beta-3 adrenergic receptors in fat cells facilitates the breakdown of stored fat, offering a potential therapeutic approach to weight management and related health issues.
Used in Metabolic Disorder Treatment:
In the field of metabolic research, 4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol is used as a potential therapeutic agent for improving glucose and lipid metabolism. Its ability to influence these metabolic pathways positions it as a candidate for the treatment of conditions such as diabetes and dyslipidemia.
Used in Obesity Treatment:
4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol is used as a potential treatment for obesity, leveraging its capacity to stimulate beta-3 adrenergic receptors and promote the breakdown of fat. This mechanism could contribute to weight loss and the mitigation of obesity-related health complications.
Further research is necessary to fully elucidate the mechanisms of action and potential side effects of 4-Chloro-3H-imidazo[4,5-c]pyridin-2-ol, ensuring its safe and effective application in clinical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 54221-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54221-73:
(7*5)+(6*4)+(5*2)+(4*2)+(3*1)+(2*7)+(1*3)=97
97 % 10 = 7
So 54221-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClN3O/c7-5-4-3(1-2-8-5)9-6(11)10-4/h1-2H,(H2,9,10,11)

54221-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one

1.2 Other means of identification

Product number -
Other names 4-Chlor-1,3-dihydro-2H-imidazo<4,5-c>-2-pyridon

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:54221-73-7 SDS

54221-73-7Relevant academic research and scientific papers

Aza-BODIPY Route to Ageladine A

Fresia, Marvin,Lindel, Thomas,Tolle, Christian

supporting information, p. 1308 - 1312 (2022/02/23)

The marine natural product ageladine A was synthesized by exploiting novel aza-BODIPY-type boron complexes that allowed the regioselective dibromination of the pyrrole unit, as confirmed by quantum chemical calculation (ωB97XD/TApr-cc-pVDZ). The parent tricycle was accessed by Suzuki-Miyaura cross-coupling employing Buchwald’s precatalyst. The boron complex of ageladine A exhibited strong fluorescence that was greater than that of the natural product by a factor of ~30 and that disappeared in the presence of 2-azido groups.

PHENYLUREA DERIVATIVES USED AS INHIBITORS OF TYROSINKINASE FOR TREATING TUMORS

-

Page/Page column 59-60, (2008/06/13)

The invention relates to the compounds of formula (I), wherein R1a-R1e, R2a, R2b, R3 and X are defined as in claim 1. The inventive derivatives are tyrosinkinase inhibitors, especially inhibitors of TIE-2, and Raf kinase inhibitors and may inter alia be used for treating tumors.

SYNTHESIS AND PROPERTIES OF 4-HALOIMIDAZOPYRIDIN-2-ONES

Yutilov, Yu.M.,Svertilova, I.A.

, p. 923 - 927 (2007/10/02)

The nitro group in 4-nitroimidazopyridin-2-ones is rather labile and may be reploaced upon heating with hydrohalic acids to give the corresponding 4-halides.A methyl group at N(3) leads to a sharp increase in the lability of the nitro gr

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