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1H-Pyrrolo[2,3-b]pyridine-3-carboxaldehyde, 1-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155819-08-2

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155819-08-2 Usage

Chemical class

pyrido[2,3-b]pyrroles

Type of compound

carboxaldehyde derivative

Substitution

sulfonyl group on the 1-position of the pyrrolopyridine ring

Check Digit Verification of cas no

The CAS Registry Mumber 155819-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,1 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155819-08:
(8*1)+(7*5)+(6*5)+(5*8)+(4*1)+(3*9)+(2*0)+(1*8)=152
152 % 10 = 2
So 155819-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O3S/c17-10-11-9-16(14-13(11)7-4-8-15-14)20(18,19)12-5-2-1-3-6-12/h1-10H

155819-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)pyrrolo[2,3-b]pyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-PYRROLO[2,3-B]PYRIDINE-3-CARBOXALDEHYDE,1-(PHENYLSULFONYL)

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:155819-08-2 SDS

155819-08-2Relevant articles and documents

A rapid method toward the synthesis of new substituted tetrahydro α-carbolines and α-carbolines

Chavan, Neelam L.,Nayak, Sandip K.,Kusurkar, Radhika S.

experimental part, p. 1827 - 1831 (2010/04/06)

A rapid and efficient method for stereoselective synthesis of new substituted tetrahydro-α-carbolines using Diels-Alder reaction under microwave irradiation has been developed. Further, dehydrogenation of these adducts resulted in synthesis of new substit

Synthesis and CDK2 kinase inhibitory activity of 7/7′-azaindirubin derivatives

Wang, Zhao Hui,Dong, Ying,Wang, Tao,Shang, Ming Hong,Hua, Wei Yi,Yao, Qi Zheng

scheme or table, p. 297 - 300 (2010/12/19)

A series of novel 7′-azaindirubin (1a-g) and 7-azaindirubin (2a, 2c, 2e and 2f) derivatives were designed and synthesized. Their structures were characterized by 1H NMR and MS spectroscopy as well as by elemental analysis. Their inhibitory properties against CDK2/cylinA were evaluated in vitro. In contrast to indirubin, some of the described azaindirubins emerged as potent inhibitors of CDK2/cylinA and compound 2b had more potent activity. Biological tests also showed that nitrogen atom at 7-position of azaindirubin was more beneficial to enhance the kinase inhibitory activity.

COMPOUNDS HAVING 5-HT6 RECEPTOR AFFINITY

-

Page/Page column 116-117, (2010/11/28)

The present disclosure provides compounds having affinity for the 5HT6 receptor which are of the formula (I), wherein R1-R3 A, B, D, E, G, Q, and x are as defined herein. The disclosure also relates to methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

Synthesis of benzo[5',6']cyclohepta[4,5]pyrrolo[2,3-b]pyridin-12-one

Mouaddib, Abderrahim,Joseph, Benoit,Hasnaoui, Aissa,Merour, Jean-Yves

, p. 5853 - 5854 (2007/10/03)

The synthesis of a 7-azaindole derivative 8 with potential antitumoral activity is described starting from pyrrolo[2,3-b]pyridine; regioselective lithiation/methylation of alkyl 7-azaindole-3-carboxylates 4 afforded the 2- methyl derivatives 5. Demethylat

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