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1-(5-Methoxy-6-nitroindolin-1-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23772-37-4

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23772-37-4 Usage

Appearance

Yellow crystalline solid

Usage

Primarily used in organic synthesis and pharmaceutical research

Potential applications

Development of new drugs and compounds for various medical purposes

Category

Indole derivative

Biological activities

Possess a wide range of biological activities, including anti-inflammatory, antimicrobial, and anticancer properties

Structure

Unique structure that makes it a valuable tool for scientists and researchers in the field of medicinal chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 23772-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23772-37:
(7*2)+(6*3)+(5*7)+(4*7)+(3*2)+(2*3)+(1*7)=114
114 % 10 = 4
So 23772-37-4 is a valid CAS Registry Number.

23772-37-4SDS

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-(5-methoxy-6-nitro-2,3-dihydroindol-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(5-Methoxy-6-nitroindolin-1-yl)ethanone

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:23772-37-4 SDS

23772-37-4Relevant academic research and scientific papers

Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Chamberlain, Stanley D.,Redman, Aniko M.,Wilson, Joseph W.,Deanda, Felix,Shotwell, J. Brad,Gerding, Roseanne,Lei, Huangshu,Yang, Bin,Stevens, Kirk L.,Hassell, Anne M.,Shewchuk, Lisa M.,Leesnitzer, M. Anthony,Smith, Jeffery L.,Sabbatini, Peter,Atkins, Charity,Groy, Arthur,Rowand, Jason L.,Kumar, Rakesh,Mook Jr., Robert A.,Moorthy, Ganesh,Patnaik, Samarjit

scheme or table, p. 360 - 364 (2011/03/18)

The SAR of C5′ functional groups with terminal basic amines at the C6 aniline of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidines is reported. Examples demonstrate potent inhibition of IGF-1R with 1000-fold selectivity over JNK1 and 3 in enzymatic assays.

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