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4-(Cyclohexylthio)-3-nitrobenzaldehyde is an organosulfur compound that is a type of sulfide. It is an aromatic compound due to the presence of a benzene ring in its structure. This chemical compound is characterized by the presence of a cyclohexylthio group, a nitro group, and a benzaldehyde group in its molecular structure. Its properties and reactivity are largely determined by these structural features.

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  • 270262-95-8 Structure
  • Basic information

    1. Product Name: 4-(CYCLOHEXYLTHIO)-3-NITROBENZALDEHYDE
    2. Synonyms: 4-(CYCLOHEXYLSULFANYL)-3-NITROBENZENECARBALDEHYDE;4-(CYCLOHEXYLTHIO)-3-NITROBENZALDEHYDE
    3. CAS NO:270262-95-8
    4. Molecular Formula: C13H15NO3S
    5. Molecular Weight: 265.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 270262-95-8.mol
  • Chemical Properties

    1. Melting Point: 98-99
    2. Boiling Point: 411.9°Cat760mmHg
    3. Flash Point: 202.9°C
    4. Appearance: /
    5. Density: 1.26g/cm3
    6. Vapor Pressure: 5.41E-07mmHg at 25°C
    7. Refractive Index: 1.598
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(CYCLOHEXYLTHIO)-3-NITROBENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(CYCLOHEXYLTHIO)-3-NITROBENZALDEHYDE(270262-95-8)
    12. EPA Substance Registry System: 4-(CYCLOHEXYLTHIO)-3-NITROBENZALDEHYDE(270262-95-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 270262-95-8(Hazardous Substances Data)

270262-95-8 Usage

Uses

Used in Chemical Synthesis:
4-(Cyclohexylthio)-3-nitrobenzaldehyde is used as a reactant or an intermediate in chemical syntheses. Its unique molecular structure with a cyclohexylthio group, a nitro group, and a benzaldehyde group makes it a valuable compound in the field of chemistry.
Used in Scientific Research:
4-(Cyclohexylthio)-3-nitrobenzaldehyde is often used in scientific research, where its properties and reactivity can be studied and utilized for various purposes. Its potential applications in this field are primarily in the realm of chemistry, where it can contribute to the development of new compounds and materials.
Note: As the provided materials mention that details about the toxicity and safety measures of 4-(Cyclohexylthio)-3-nitrobenzaldehyde are not widely available, it is essential to conduct further studies to understand its potential risks and safety measures before widespread use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 270262-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,6 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 270262-95:
(8*2)+(7*7)+(6*0)+(5*2)+(4*6)+(3*2)+(2*9)+(1*5)=128
128 % 10 = 8
So 270262-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3S/c15-9-10-6-7-13(12(8-10)14(16)17)18-11-4-2-1-3-5-11/h6-9,11H,1-5H2

270262-95-8SDS

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 4-cyclohexylsulfanyl-3-nitrobenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(Cyclohexylthio)-3-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:270262-95-8 SDS

270262-95-8Upstream product

270262-95-8Downstream Products

270262-95-8Relevant articles and documents

Expanding the scope of human DNA polymerase and inhibitors

Strittmatter, Tobias,Brockmann, Anette,Pott, Moritz,Hantusch, Annika,Brunner, Thomas,Marx, Andreas

, p. 282 - 290 (2014/06/09)

The exact biological functions of individual DNA polymerases still await clarification, and therefore appropriate reagents to probe their respective functions are required. In the present study, we report the development of a highly potent series of human DNA polymerase γand β(pol γandβ ) inhibitors based on the rhodanine scaffold. Both enzymes are involved in DNA repair and are thus considered as future drug targets. We expanded the chemical diversity of the small-molecule inhibitors arising from a high content screening and designed and synthesized 30 novel analogues. By biochemical evaluation, we discovered 23 highly active compounds against polβ . Importantly, 10 of these small-molecules selectively inhibited polβ and not the homologous polβ . We discovered 14 small-molecules that target polγ and found out that they are more potent than known inhibitors. We also investigated whether the discovered compounds sensitize cancer cells toward DNAdamaging reagents. Thus, we cotreated human colorectal cancer cells (Caco-2) with the small-molecule inhibitors and hydrogen peroxide or the approved drug temozolomide. Interestingly, the tested compounds sensitized Caco-2 cells to both genotoxic agents in a DNA repair pathway-dependent manner.2013 American Chemical Society.

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