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52505-41-6

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52505-41-6 Usage

Appearance

Yellow solid

Usage

Commonly used in research and laboratory settings

Derivative of

Thieno[2,3-b]pyridine

Contains functional groups

Amino group and ketone group

Useful for

Various chemical reactions and processes

Potential applications

Pharmaceuticals, agrochemicals, and material science

Biological activity

Being investigated for potential use in drug development

Importance

Range of potential applications in scientific and industrial fields

Check Digit Verification of cas no

The CAS Registry Mumber 52505-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,0 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52505-41:
(7*5)+(6*2)+(5*5)+(4*0)+(3*5)+(2*4)+(1*1)=96
96 % 10 = 6
So 52505-41-6 is a valid CAS Registry Number.

52505-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Aminothieno[2,3-b]pyridin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-acetyl-3-aminothiopheno[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:52505-41-6 SDS

52505-41-6Downstream Products

52505-41-6Relevant articles and documents

Straightforward synthesis of 2-acetyl-substituted benzo[b]thiophenes

Debray, Julien,Lemaire, Marc,Popowycz, Florence

, p. 37 - 40 (2013/02/23)

Described herein is a green one-step protocol for the preparation of substituted 2-acetylbenzo[b]thiophenes from commercially available aromatic halides. This efficient method has the advantage of using water as the reaction medium, resulting in a high yield of pure cyclized products. Two scaffold types have been prepared using this general procedure: 2-acetylbenzo[b]thiophenes and 2-acetyl-3-aminobenzo[b]thiophenes, both crystallized directly from the reaction mixture, due to their low solubility with water, and without the need for an additional purification step. Georg Thieme Verlag Stuttgart · New York.

Synthesis of 3 aminothieno [2,3 b]pyridine derivatives II

Guerrera,Siracusa,Tornetta

, p. 21 - 30 (2007/10/05)

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