101033-02-7

Basic information

• Product Name: 1,3-Dithiolane, 2-(2-nitrophenyl)-
• CAS NO: 101033-02-7
• Molecular Formula: C9H9NO2S2
• Molecular Weight: 227.308
• Mol File: 101033-02-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1,3-Dithiolane, 2-(2-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dithiolane, 2-(2-nitrophenyl)-(101033-02-7)
• EPA Substance Registry System: 1,3-Dithiolane, 2-(2-nitrophenyl)-(101033-02-7)

Safety Data

• Hazardous Substances Data: 101033-02-7(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C), 9 hydrogen (H), 1 nitrogen (N), 2 oxygen (O), and 2 sulfur (S) atoms.

Explanation

Heterocyclic compounds are organic compounds containing a ring of atoms, with at least one atom in the ring being different from carbon. In this case, the compound has a dithiolane ring (a four-membered ring with two sulfur atoms and two carbon atoms).

Explanation

The dithiolane ring is the core structure of the compound, consisting of a four-membered ring with two sulfur atoms and two carbon atoms.

Explanation

The compound is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is also utilized in organic synthesis and research due to its unique chemical properties.

Explanation

Due to its potential hazards, it is essential to handle this compound with care to avoid any adverse effects on health or the environment.

Explanation

The stability of the compound can be influenced by factors such as temperature, light exposure, and the presence of other reactive substances. Proper storage and handling are crucial to maintain its stability and prevent degradation.

Structure

Heterocyclic organic compound

Dithiolane Ring

Contains two sulfur atoms and two carbon atoms

2-Nitrophenyl Group

Attached to one of the sulfur atoms

Applications

Pharmaceutical intermediate, agrochemicals, dyes, organic synthesis, and research

Hazardous Nature

Requires careful handling

Chemical Stability

May vary depending on storage and handling conditions

Upstream product

• 42526-65-8 2-(2-nitrophenyl)-1,3-dioxane 
• 540-63-6 ethane-1,2-dithiol 
• 48140-35-8 2-(2-nitrophenyl)-1,3-dioxolane 
• 88356-11-0 o-nitrobenzaldehyde diethylacetal 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 1476042-37-1 3-(2-(2-nitrophenyl)-1,3-dithiolan-2-yl)-1H-indole 

Relevant articles and documents

Ruthenium(III) chloride-catalyzed thioacetalization of carbonyl compounds: Scope, selectivity, and limitations

A variety of carbonyl compounds can be easily and rapidly converted to the corresponding cyclic and acylic dithioacetals in the presence of a catalytic amount of ruthenium chloride in acetonitrile at room temperature. Some of the major advantages of this

Solvent free thioacetalization of carbonyl compounds catalyzed by Cu(OTf)2-SiO2

Aldehydes and ketones were thioacetalyzed using 1,2-ethanedithiol in the presence of a catalytic amount of Cu(OTf)2-SiO2 under solvent free conditions in excellent yields.

Sulfonated polyanthracene-catalyzed highly efficient and chemoselective thioacetalization of carbonyl compounds and transthioacetalization of acetals and acylals

A straightforward and highly efficient procedure for the thioacetalization of a variety of aldehydes and transthioacetalization of acylals and acetals in good to excellent yields using catalytic amounts of sulfonated polyanthracene (S-PAT) is reported. Th

Aluminum hydrogen sulfate [Al(HSO4)3] as an efficient catalyst for the preparation of thioacetals

Aluminum hydrogen sulfate, as a heterogeneous solid acid catalyst, has been used for the mild conversion of carbonyl compounds to their thioacetals using 1,2- and 1,3-dithiol under ambient conditions with short reaction times in high to excellent yield in

An efficient method for the transthioacetalization of acylals and acetals under mild conditions

A rapid and efficient method for the transthioacetalization of acylals (1,1-diacetates) and acyclic and cyclic acetals is described. The reaction was carried out using 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane tribromide (1 mol%). The yield of the transthioacetalization was high and reaction conditions involve the use of acetonitrile as the solvent at room temperature; isolation is simple and the products are nearly pure.