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5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE is a chemical compound characterized by the molecular formula C12H8N2O3S. It is a nitroaromatic compound that features a nitro group and a pyridylthio group attached to a benzaldehyde moiety. 5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE is recognized for its chemical properties and reactivity, which make it a valuable building block in the preparation of complex organic molecules. Due to its potential hazards, safety precautions are essential when handling 5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE to prevent harm from ingestion, inhalation, or contact with skin or eyes.

175278-54-3

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175278-54-3 Usage

Uses

Used in Organic Synthesis:
5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE is utilized as a reagent in various organic synthesis processes. Its unique structure and reactivity contribute to the formation of a wide range of complex organic molecules, making it an indispensable component in the synthesis of new compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE serves as an intermediate in the synthesis of diverse pharmaceutical compounds. Its role in the development of new drugs is significant, as it can be incorporated into the molecular structures of potential therapeutic agents.
Used in Chemical Reactions:
5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE is also employed in a variety of chemical reactions, where its nitro and pyridylthio groups participate in different types of chemical transformations. This versatility allows it to be a key player in the synthesis of a broad spectrum of chemical products.
Used in Research and Development:
Due to its unique chemical properties, 5-NITRO-2-(2-PYRIDYLTHIO)BENZALDEHYDE is often used in research and development settings to explore new chemical reactions, investigate its reactivity, and understand its potential applications in various fields, including material science and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 175278-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,7 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175278-54:
(8*1)+(7*7)+(6*5)+(5*2)+(4*7)+(3*8)+(2*5)+(1*4)=163
163 % 10 = 3
So 175278-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N2O3S/c15-8-9-7-10(14(16)17)4-5-11(9)18-12-3-1-2-6-13-12/h1-8H

175278-54-3SDS

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 5-nitro-2-pyridin-2-ylsulfanylbenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:175278-54-3 SDS

175278-54-3Downstream Products

175278-54-3Relevant academic research and scientific papers

Nitroarylhydroxymethylphosphonic acids as inhibitors of CD45

Beers, Scott A.,Malloy, Elizabeth A.,Wu, Wei,Wachter, Michael P.,Gunnia, Uma,Cavender, Druie,Harris, Crafford,Davis, Janet,Brosius, Ruth,Pellegrino-Gensey, J. Lee,Siekierka, John

, p. 2203 - 2211 (2007/10/03)

A series of nitroarylhydroxymethylphosphonic acids was synthesized and evaluated as inhibitors of CD45. It was discovered that both the alpha hydroxy and nitro groups are essential for activity. Potency is enhanced by the addition of a large lipophilic group on the aryl ring adjacent to the phosphonic acid moiety. Kinetics studies have shown that these compounds are competitive inhibitors and thus bind at the active site of this enzyme.

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