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2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE is a chemical compound characterized by the molecular formula C13H15NO3S. It is a yellow crystalline solid that exhibits a distinctive odor. 2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE is notable for its chemical structure, which includes a nitro group and a thioether, endowing it with versatility as a building block in the synthesis of a diverse range of organic compounds. Its potential biological activity, particularly as an antimicrobial and antitumor agent, has also been a subject of study. However, due to its toxic nature and the potential for skin and eye irritation upon contact, it requires careful handling and use.

175278-46-3

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175278-46-3 Usage

Uses

Used in Organic Synthesis:
2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE is utilized as a reagent in organic synthesis for its ability to contribute to the formation of various organic compounds. Its unique structure with a nitro group and a thioether allows it to participate in a wide array of chemical reactions, making it a valuable component in the synthesis process.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE serves as a building block in the creation of different medicinal compounds. Its chemical properties facilitate its integration into the structures of potential drugs, contributing to the development of new therapeutic agents.
Used in Agrochemical Production:
Similarly, in agrochemicals, 2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE is employed as a building block for the production of various agrochemicals. Its role in these products is crucial for the development of effective compounds used in agriculture to protect crops and enhance yields.
Used in Antimicrobial Applications:
2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE has been studied for its potential as an antimicrobial agent. Its ability to combat microorganisms makes it a candidate for use in applications where control of microbial growth is necessary, such as in medical or environmental settings.
Used in Antitumor Applications:
2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE has also been investigated for its potential antitumor activity. Research into its capacity to inhibit tumor growth and its possible use in cancer treatment underscores another area where 2-(CYCLOHEXYLTHIO)-5-NITROBENZALDEHYDE could be applied, further expanding its utility in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 175278-46-3 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, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175278-46:
(8*1)+(7*7)+(6*5)+(5*2)+(4*7)+(3*8)+(2*4)+(1*6)=163
163 % 10 = 3
So 175278-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3S/c15-9-10-8-11(14(16)17)6-7-13(10)18-12-4-2-1-3-5-12/h6-9,12H,1-5H2

175278-46-3SDS

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 2-cyclohexylsulfanyl-5-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-(cyclohexylsulfanyl)-5-nitrobenzaldehyde

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:175278-46-3 SDS

175278-46-3Relevant 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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