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5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE is a chemical compound with the molecular formula C13H9NO3S. It is a nitrobenzaldehyde derivative that features a nitro group and a phenylthio group. 5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE is known for its potential as a building block in organic synthesis, contributing to the creation of a variety of other organic compounds.

52548-32-0

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52548-32-0 Usage

Uses

Used in Organic Synthesis:
5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE is used as a building block in organic synthesis for the creation of other organic compounds. Its unique structure, which includes both a nitro and a phenylthio group, allows for a wide range of reactions and the synthesis of diverse chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE is used as an intermediate in the synthesis of pharmaceuticals. The presence of the nitro group makes it a versatile intermediate for the development of various medicinal compounds, potentially leading to new drugs with different therapeutic properties.
Used in Agrochemicals:
5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE also finds application in the agrochemical sector, where it serves as a precursor for the synthesis of agrochemicals. Its ability to participate in various chemical reactions makes it a valuable component in the development of new pesticides or other agricultural chemicals.
Used in Materials Science:
In the field of materials science, 5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE is utilized for the development of new materials. Its chemical structure may contribute to the creation of materials with unique properties, such as improved stability or specific interactions with other molecules.
Potential Use as a Pharmacological Agent:
Given its chemical structure, 5-NITRO-2-(PHENYLTHIO)BENZALDEHYDE could have biological activity, suggesting a potential use as a pharmacological agent. Further research would be required to explore its specific biological effects and therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 52548-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52548-32:
(7*5)+(6*2)+(5*5)+(4*4)+(3*8)+(2*3)+(1*2)=120
120 % 10 = 0
So 52548-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO3S/c15-9-10-8-11(14(16)17)6-7-13(10)18-12-4-2-1-3-5-12/h1-9H

52548-32-0SDS

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 5-nitro-2-phenylsulfanylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-Nitro-2-phenylmercapto-benzaldehyd

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:52548-32-0 SDS

52548-32-0Relevant 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.

10,11-Dihydro-dibenzo(b,f)thiepin derivatives

-

, (2016/03/01)

Dibenzothiepin derivatives of the general formula STR1 wherein m, n, R1, R2, R3 and X are as hereinafter set forth, And salts thereof as well as processes for their manufacture are disclosed. The end products are useful as central-depressant and neuroleptic agents.

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