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1011711-52-6

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1011711-52-6 Usage

General Description

Ethanone, 1-(4-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)- is a chemical compound with the molecular formula C10H7ClN2O. It is a synthetic organic compound that is used in the field of medicinal chemistry for the development of potential pharmaceutical drugs. The compound contains a chlorine atom and a pyrrolo[2,3-b]pyridine ring structure, making it a heterocyclic compound. This unique structure may contribute to its potential pharmacological properties, making it an interesting target for further research and development. Its potential applications include as a drug intermediate or as a research tool in the study of biological pathways and disease mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 1011711-52-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,7,1 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1011711-52:
(9*1)+(8*0)+(7*1)+(6*1)+(5*7)+(4*1)+(3*1)+(2*5)+(1*2)=76
76 % 10 = 6
So 1011711-52-6 is a valid CAS Registry Number.

1011711-52-6SDS

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 1-(4-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 3-acetyl-4-chloro-1H-pyrrolo[2,3-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:1011711-52-6 SDS

1011711-52-6Relevant articles and documents

Room-Temperature and Transition-Metal-Free Intramolecular α-Arylation of Ketones: A Mild Access to Tetracyclic Indoles and 7-Azaindoles

Adouama, Chérif,Budén, María E.,Guerra, Walter D.,Puiatti, Marcelo,Joseph, Beno?t,Barolo, Silvia M.,Rossi, Roberto A.,Médebielle, Maurice

, (2018)

A novel approach for the synthesis of tetracyclic indoles and 7-azaindoles is reported. The strategy involves four steps, with a fast rt intramolecular α-arylation of ketones as key step. The reaction was inspected synthetically to achieve the synthesis of 11 novel tetracyclic structures with moderate to very good yields (39-85%). Theoretical combined with experimental studies led us to propose a probable polar mechanism (concerted SNAr).

Room-Temperature and Transition-Metal-Free Intramolecular α-Arylation of Ketones: A Mild Access to Tetracyclic Indoles and 7-Azaindoles

Adouama, Chérif,Budén, María E.,Guerra, Walter D.,Puiatti, Marcelo,Joseph, Beno?t,Barolo, Silvia M.,Rossi, Roberto A.,Médebielle, Maurice

supporting information, p. 320 - 324 (2019/01/10)

A novel approach for the synthesis of tetracyclic indoles and 7-azaindoles is reported. The strategy involves four steps, with a fast rt intramolecular α-arylation of ketones as key step. The reaction was inspected synthetically to achieve the synthesis of 11 novel tetracyclic structures with moderate to very good yields (39-85%). Theoretical combined with experimental studies led us to propose a probable polar mechanism (concerted SNAr).

PYRROLO[2,3-B]PYRIDINE COMPOUNDS, AZAINDOLE COMPOUNDS USED FOR SYNTHESIZING SAID PYRROLO[2,3-B]PYRIDINE COMPOUNDS, METHODS FOR THE PRODUCTION THEREOF, AND USES THEREOF

-

Page/Page column 6, (2010/08/07)

The invention relates to pyrrolo[2,3-b]pyridine compounds and azaindole compounds used for the synthesis thereof. The invention also relates to methods for the production thereof and the uses thereof. Said novel pyrrolo[2,3-b]pyridine compounds according to the invention have great antiproliferative, apoptotic, and neuroprotective activities. The invention particularly applies to the pharmaceutical field.

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