16862-05-8

Basic information

• Product Name: Methyl-3-(2-thienyl)=propionate
• Synonyms: Methyl-3-(2-thienyl)=propionate;2-Thiophenepropanoicacid,methylester;3-(Thiophen-2-yl)propionic Acid Methyl Ester;Methyl 3-(thiophen-2-yl)propanoate
• CAS NO: 16862-05-8
• Molecular Formula: C₈H₁₀O₂S
• Molecular Weight: 170.2288
• Product Categories: Aromatics;Sulfur & Selenium Compounds
• Mol File: 16862-05-8.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 228.2 °C at 760 mmHg
• Flash Point: 91.8 °C
• Appearance: /
• Density: 1.148g/cm³
• Vapor Pressure: 0.0744mmHg at 25°C
• Refractive Index: 1.522
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Methyl-3-(2-thienyl)=propionate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-3-(2-thienyl)=propionate(16862-05-8)
• EPA Substance Registry System: Methyl-3-(2-thienyl)=propionate(16862-05-8)

Safety Data

• Hazardous Substances Data: 16862-05-8(Hazardous Substances Data)

Usage

Description

Methyl 3-(2-Thienyl)propanoate, with the CAS number 16862-05-8, is a colorless oil compound that is useful in organic synthesis. It is an organic compound with a thienyl group attached to a propanoate group, which contributes to its unique chemical properties and potential applications in various industries.

Uses

1. Used in Organic Synthesis:
Methyl 3-(2-Thienyl)propanoate is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block for the creation of more complex molecules, which can be utilized in different applications such as pharmaceuticals, agrochemicals, and materials science.
2. Used in Pharmaceutical Industry:
Methyl 3-(2-Thienyl)propanoate is used as a key component in the development of new pharmaceutical compounds. Its unique chemical structure can be exploited to design and synthesize novel drugs with potential therapeutic applications, such as those targeting specific diseases or conditions.
3. Used in Agrochemical Industry:
In the agrochemical industry, Methyl 3-(2-Thienyl)propanoate can be used as a starting material for the synthesis of new pesticides, herbicides, or other crop protection agents. Its unique properties may contribute to the development of more effective and environmentally friendly products.
4. Used in Materials Science:
Methyl 3-(2-Thienyl)propanoate can also be utilized in the development of new materials with specific properties, such as improved conductivity, stability, or other characteristics. Its unique structure can be incorporated into the design of advanced materials for various applications, including electronics, energy storage, and more.

InChI:InChI=1/C8H10O2S/c1-10-8(9)5-4-7-3-2-6-11-7/h2-3,6H,4-5H2,1H3

Upstream product

• 5928-51-8 3-(2-thienyl)propanoic acid 
• 79-22-1 methyl chloroformate 
• 67-56-1 methanol 
• 15690-25-2 3-(2-thienyl)acrylic acid 
• 77998-66-4 C₄H₃S^(1-) 
• 292638-85-8 acrylic acid methyl ester 
• 26359-21-7 3-(thiophen-2-yl)propanal 
• 1124-65-8 3-(2-thienyl)-2-propenoic acid 
• 5834-04-8 3-(2-thienyl)-propanoic acid chloride 
• 57502-38-2 methyl (E)-3-(2-thienyl)propenoate 

Downstream Products

• 19498-72-7 3-thiophen-2-yl-propan-1-ol 
• 5650-51-1 5,6-dihydro-<6H>-cyclopenta--thiophene-4-one 
• 954238-22-3 5,6-dihydro-4H-cyclopenta[b]thiophen-4-ol 
• 133486-21-2 (E)-3-[2-n-butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)methyl-2-propenol 
• 133486-11-0 (E)-3-[2-n-butyl-1-[(2-chlorophenyl)methyl]-1H-imidazol-5-yl]-2-(thien-2-yl)methyl-2-propenamide 
• 148674-39-9 SB 206328 

Relevant articles and documents

Organopalladium approaches to prostaglandins. I. Synthesis of thiophene-containing prostaglandin endoperoxide analogs via thienylpalladation of bicyclic olefins

-

Organopalladium approaches to prostaglandins. 5. Synthesis of bicyclic and tricyclic prostanoic acids and thiophene-containing prostaglandin endoperoxide analogues via thienylpalladation of bicyclic alkenes

-

Industrial preparation method of 2-ethylamine-heterocyclic derivative

The invention provides an industrial preparation method of a 2-ethylamine-heterocyclic derivative. The method is characterized in that a heteroaryl derivative and 2-substituent ethylene react to produce a 2-(2-cyanoethyl)-heterocyclic derivative, a 2-acetate-heterocyclic derivative and a 2-(3-butyl ketone)-heterocyclic derivative separately. The production method is simple and different from complicated production modes and harsh production conditions in the prior art. By means of the industrial preparation method, synthesis of a target product can be achieved by one step. As the production technology and synthetic route are optimized through the preparation method, in the production process, few side reactions occur, the aftertreatment is convenient, the production condition is mild, and the preparation method is suitable for an industrialized production mode.

Visible light-induced selective generation of radicals from organoborates by photoredox catalysis

A new strategy for the generation of carbon-centered radicals via oxidation of alkyl-, allyl-, benzyl- and arylborates by visible-light-driven single electron transfer (SET) photoredox catalysis has been established. The generated radicals smoothly react with TEMPO and electron-deficient alkenes to afford C-O and C-C coupling products, respectively. In this radical initiating system, cyclic organo(triol)borates turn out to be useful radical precursors.