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1-(Hexylsulfanyl)-2,4-dinitrobenzene is an organic compound characterized by a benzene ring with two nitro groups at the 2nd and 4th positions and a hexylsulfanyl group attached to the 1st position. 1-(hexylsulfanyl)-2,4-dinitrobenzene is known for its unique chemical structure, which combines the properties of an aromatic ring with the reactivity of a sulfanyl group. The hexylsulfanyl group, consisting of a sulfur atom bonded to a hexyl chain, introduces a lipophilic character to the molecule, potentially affecting its solubility and reactivity. The presence of two nitro groups enhances the compound's reactivity and may lead to the formation of various derivatives through substitution reactions. This chemical's properties make it a subject of interest in organic chemistry, particularly in the synthesis of complex molecules and the study of aromatic substitution patterns.

7343-59-1

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7343-59-1 Usage

Chemical class

Dinitrobenzene derivatives

Structure

Benzene ring with two nitro groups (-NO2) and a hexylsulfanyl group (-S-(CH2)5CH3) attached

Functional groups

Nitro groups, Sulfonyl group

Applications

a. Organic synthesis
b. Precursor or intermediate in chemical production
c. Development of pharmaceuticals
d. Development of agrochemicals

Toxicity

Toxic, should be handled with caution

Physical state

Likely a solid (based on similar compounds)

Solubility

Likely soluble in organic solvents (e.g., ethanol, acetone) due to the presence of a nonpolar hexyl chain

Stability

May be sensitive to heat, light, or moisture due to the presence of nitro groups

Reactivity

Reactive towards nucleophiles and reducing agents due to the presence of nitro groups

Hazards

Potential health hazards (respiratory, skin, eye irritation) and environmental hazards (aquatic toxicity, soil contamination) due to its toxicity and chemical structure

Check Digit Verification of cas no

The CAS Registry Mumber 7343-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7343-59:
(6*7)+(5*3)+(4*4)+(3*3)+(2*5)+(1*9)=101
101 % 10 = 1
So 7343-59-1 is a valid CAS Registry Number.

7343-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexylsulfanyl-2,4-dinitrobenzene

1.2 Other means of identification

Product number -
Other names Sulfide,2,4-dinitrophenyl hexyl

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:7343-59-1 SDS

7343-59-1Relevant academic research and scientific papers

Short Wavelength Inner Filter Technique (SWIFT) in Designing Reactive Fluorescent Molecular Probes

Baheti, Abhishek,Vigalok, Arkadi

, p. 12224 - 12228 (2019/08/21)

Here, we present a conceptually novel and experimentally straightforward technique for selective analyte detection that uses a combination of commercial fluorophores and simple chemicals. The technique utilizes the well-known inner filter effect (IFE); however, the fluorophore's excitation is performed at wavelengths significantly shorter than its absorption maximum. In the presence of the analyte, the "filter" appears or disappears at the excitation wavelength resulting in the fluorescence turning OFF or ON, respectively. Unlike common probes, our technique allows real-time monitoring of a fluorophore's stability as well as its recycling. We further demonstrate the applicability of this technique in continuing analyte detection as well as vapor analysis.

Synthesis of 4-nitrophenyl sulfones and application in the modified Julia olefination

Mirk, Daniela,Grassot, Jean-Marie,Zhu, Jieping

, p. 1255 - 1259 (2007/10/03)

4-Nitrophenyl (NP) sulfones have been successfully employed in the modified Julia olefination reaction with carbonyl compounds. The olefination reaction proceeds through a sequence of aldol addition, Smiles rearrangement, and elimination. The sulfones are easily prepared in high yields in a two-step sequence starting from inexpensive commercially available para- fluoronitrobenzenes via nucleophilic aromatic substitution by a mercaptane and subsequent oxidation under standard conditions. The modified Julia reaction between NP sulfones and a wide variety of aromatic aldehydes affords the corresponding styrenes, stilbenes and cinnamate derivatives in yields up to 97% and good stereoselectivities. A mechanistic rationale is advanced to explain the observed results. Georg Thieme Verlag Stuttgart.

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