40412-09-7

Basic information

• Product Name: 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate
• Synonyms: 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate
• CAS NO: 40412-09-7
• Molecular Formula: C₁₃H₁₄O₃S₂
• Molecular Weight: 282.37846
• Mol File: 40412-09-7.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate(40412-09-7)
• EPA Substance Registry System: 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate(40412-09-7)

Safety Data

• Hazardous Substances Data: 40412-09-7(Hazardous Substances Data)

Usage

General Description

2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate is a chemical compound with the molecular formula C15H16O3S2. It is composed of a thiophene ring attached to an ethyl group and a 4-methylbenzenesulfonate group. 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate is commonly used in organic synthesis as a reagent for introducing sulfonate groups into organic molecules. It is also used in pharmaceutical and agrochemical industries as a building block for the synthesis of various bioactive compounds. Additionally, it has potential applications in material science and polymer chemistry due to its ability to modify the physical and chemical properties of materials. Overall, 2-(thiophen-3-yl)ethyl 4-methylbenzenesulfonate is a versatile and important compound with a wide range of potential uses in different fields.

Upstream product

• 13781-67-4 3-(2-hydroxyethyl)thiophene 
• 98-59-9 p-toluenesulfonyl chloride 
• 6964-21-2 thiophen-3-yl-acetic acid 

Downstream Products

• 143035-74-9 2,9-bis(p-(2-(3-thienyl)ethan-1-oxy)phenyl)-1,10-phenanthroline 
• 79146-60-4 N-(phenyl)-N-[1-(2-(3-thienyl)ethyl)-4-methoxymethyl-4piperidinyl]propanamide 
• 79146-59-1 N-(phenyl)-N-[1-(2-(3-thienyl)ethyl)-4-methoxycarbonyl-4piperidinyl]propanamide 
• 244177-18-2 5,11,17,23-tetrakis(1,1-dimethylethyl)-25-benzyloxy-27-[2-(3-thienyl)ethoxy]-26,28-dihydroxy-calix[4]arene 
• 1263175-45-6 4-(2-(thiophen-3-yl)ethoxy)phenol 
• 1263175-43-4 C₆₅H₅₈N₄O₃S 
• 1535185-15-9 2-(2-(2-(2-(thiophen-3-yl)ethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate 
• 1451042-18-4 N-(2-aminophenyl)-4-[1-(2-thiophen-3-ylethyl)-1H-[1],[2],[3]-triazol-4-yl]benzamide 

Relevant articles and documents

Enantiomeric substituents determine the chirality of luminescent conjugated polythiophenes

Chiral isomers of 3-substituted polythiophenes with amino acid functiontionalized side chains are compared. The polymers show pH-dependent absorption, emission, and circular dichroism spectra in buffered aqueous solution. At pH equal to pi of the amino ac

ISOFORM-SELECTIVE LYSINE DEACETYLASE INHIBITORS

Isoform-selective lysine deacetylase inhibitors are described. Inhibitors of the lysine deacetylase enzyme are useful as antitumor drugs and for treating addiction, asthma, cardio-vascular disease, immunosuppression, neurodegenerative diseases, sepsis, sickle-cell disease, uveal melanoma and termination of viral latency, particularly HIV-1 latency.

Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy

A short entry to substituted azocanes by a Rh-catalyzed cycloaddition-fragmentation process is described. Specifically, exposure of diverse N-cyclopropylacrylamides to phosphine-ligated cationic Rh(I) catalyst systems under a CO atmosphere enables the directed generation of rhodacyclopentanone intermediates. Subsequent insertion of the alkene component is followed by fragmentation to give the heterocyclic target. Stereochemical studies show, for the first time, that alkene insertion into rhodacyclopentanones can be reversible.