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Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI), is a pyrrolopyridine derivative with a molecular formula of C10H8N2O and a molecular weight of 172.18 g/mol. This chemical compound features a unique structure that includes a pyrrole ring fused to a pyridine ring and contains a ketone group. It is utilized in pharmaceutical research and drug development as a potential scaffold for drug molecules due to its distinctive structural features and potential biological activity. The specific pharmacological and therapeutic properties of Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)- (9CI) are currently under investigation.

67058-71-3

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67058-71-3 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI) is employed as a potential scaffold for drug molecules in pharmaceutical research and drug development. Its unique structure and potential biological activity make it a valuable candidate for the design and synthesis of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI) is used as a starting point for the development of novel compounds with potential therapeutic applications. Its structural features can be modified and optimized to enhance the pharmacological properties and improve the efficacy of the resulting drug candidates.
Used in Drug Discovery:
Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI) is utilized in drug discovery processes to identify and develop new chemical entities with potential therapeutic benefits. Its unique structure allows for the exploration of various chemical modifications and the evaluation of its biological activity against different targets, leading to the discovery of new drugs with improved safety and efficacy profiles.
Used in Chemical Synthesis:
In chemical synthesis, Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI) serves as a key intermediate or building block for the synthesis of more complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Biological Research:
Ethanone, 1-(1H-pyrrolo[2,3-c]pyridin-3-yl)(9CI) is also used in biological research to study its interactions with various biological targets, such as enzymes, receptors, and other proteins. This research helps to understand the compound's mechanism of action and its potential therapeutic effects, paving the way for the development of new drugs with novel modes of action.

Check Digit Verification of cas no

The CAS Registry Mumber 67058-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67058-71:
(7*6)+(6*7)+(5*0)+(4*5)+(3*8)+(2*7)+(1*1)=143
143 % 10 = 3
So 67058-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-6(12)8-4-11-9-5-10-3-2-7(8)9/h2-5,11H,1H3

67058-71-3SDS

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-(1H-Pyrrolo[2,3-c]pyridin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 3-Acetyl-6-azaindol

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:67058-71-3 SDS

67058-71-3Downstream Products

67058-71-3Relevant academic research and scientific papers

Discovery and optimization of a novel series of dyrk1b kinase inhibitors to explore a MEK resistance hypothesis

Kettle, Jason G.,Ballard, Peter,Bardelle, Catherine,Cockerill, Mark,Colclough, Nicola,Critchlow, Susan E.,Debreczeni, Judit,Fairley, Gary,Fillery, Shaun,Graham, Mark A.,Goodwin, Louise,Guichard, Sylvie,Hudson, Kevin,Ward, Richard A.,Whittaker, David

, p. 2834 - 2844 (2015/04/14)

Potent and selective inhibitors of Dyrk1B kinase were developed to explore the hypothesis, based on siRNA studies, that Dyrk1B may be a resistance mechanism in cells undergoing a stress response.

An effective procedure for the acylation of azaindoles at C-3

Zhang, Zhongxing,Yang, Zhong,Wong, Henry,Zhu, Juliang,Meanwell, Nicholas A.,Kadow, John F.,Wang, Tao

, p. 6226 - 6227 (2007/10/03)

Conditions for attachment of acetyl chloride, benzoyl chloride, and chloromethyl oxalate to the 3-position of 4-, 5-, 6-, or 7-azaindoles were explored. Best results were achieved with an excess of AlCl3 in CH2Cl2 followed

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