58729-31-0

Basic information

• Product Name: ETHYL THIOMORPHOLINE-3-CARBOXYLATE
• Synonyms: THIOMORPHOLINE-3-CARBOXYLIC ACID ETHYL ESTER;(+/-)-PERHYDRO-1, 4-THIAZINE-3-CARBOXYLIC ACID ETHYL ESTER;ETHYL THIOMORPHOLINE-3-CARBOXYLATE;Thiomorpholine-3-carboxylic acid ethyl eater;Ethyl thiomorpholine-3-carboxylate 97%;3-(Ethoxycarbonyl)thiomorpholine, 3-(Ethoxycarbonyl)-1,4-thiazinane;3-Thiomorpholinecarboxylic acid ethyl ester;Ethyl 3-thiomorpholinecarboxylate
• CAS NO: 58729-31-0
• Molecular Formula: C₇H₁₃NO₂S
• Molecular Weight: 175.25
• Mol File: 58729-31-0.mol
• Article Data: 6

Chemical Properties

• Melting Point: 118 °C
• Boiling Point: 114-118℃ (7-8 Torr)
• Flash Point: 112.2 °C
• Appearance: /
• Density: 1.122 g/cm³
• Vapor Pressure: 0.011mmHg at 25°C
• Refractive Index: 1.495
• Storage Temp.: 2-8°C
• PKA: 7.26±0.40(Predicted)
• CAS DataBase Reference: ETHYL THIOMORPHOLINE-3-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL THIOMORPHOLINE-3-CARBOXYLATE(58729-31-0)
• EPA Substance Registry System: ETHYL THIOMORPHOLINE-3-CARBOXYLATE(58729-31-0)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 58729-31-0(Hazardous Substances Data)

Usage

General Description

Ethyl thiomorpholine-3-carboxylate is a chemical compound with the formula C9H17NO3S. It is a derivative of thiourea and is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. ETHYL THIOMORPHOLINE-3-CARBOXYLATE has potential applications in the field of medicine, particularly in drug development and production. Ethyl thiomorpholine-3-carboxylate is known for its diverse biological activities, including antifungal and antibacterial properties, making it a valuable component in the development of new drugs for treating various infections. Its versatile nature and potential therapeutic benefits make it an important chemical compound in the pharmaceutical and medical industries.

InChI:InChI=1/C7H13NO2S/c1-2-10-7(9)6-5-11-4-3-8-6/h6,8H,2-5H2,1H3

Upstream product

• 72850-30-7 5,6-Dihydro-2H-[1,4]thiazine-3-carboxylic acid ethyl ester 
• 70-23-5 ethyl Bromopyruvate 
• 60-23-1 Cysteamine 
• 3674-13-3 2,3-dibromopropionic acid ethyl ester 

Downstream Products

• 20960-92-3 perhydro-1,4-thiazine-3-carboxylic acid 
• 128453-98-5 thiomorpholine-3,4-dicarboxylic acid 4-tert-butyl ester 
• 156474-26-9 1-oxoperhydro-1,4-thiazine-3-carboxylic acid 
• 185382-58-5 isopropyl 3-{2-chloro-4-fluoro-5-[5,6,8,8a-tetrahydro-1,3-dioxo-1H-imidazo[5,1-c][1,4]-thiazin-2(3H)-yl]phenyl}tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate 
• 72849-62-8 2-(4-chloro-phenyl)-tetrahydro-imidazo[5,1-c][1,4]thiazine-1,3-dione 
• 72849-48-0 4-(4-chloro-2-fluoro-phenylcarbamoyl)-thiomorpholine-3-carboxylic acid ethyl ester 
• 72849-64-0 2-(2-Fluoro-4-chlorophenyl)-5,6,8,8A-tetrahydro-1H-imidazo-[5,1-c][1,4]thiazine-1,3(2H)-dione 
• 590409-08-8 4-(3-nitrobenzoyl)thiomorpholine-3-carboxylic acid ethyl ester 
• 1065333-64-3 4-(4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)thiomorpholine-3-carboxylic acid ethyl ester 
• 1065333-25-6 4-(4-(5-methyl-2-phenyloxazol-4-ylmethoxy)benzyl)thiomorpholine-3-carboxylic acid ethyl ester 
• 1065333-24-5 4-(4-(5-methyl-2-phenyloxazol-4-ylmethoxy)benzyl)thiomorpholine-3-carboxylic acid 

Relevant articles and documents

Catalytic Synthesis of N-Unprotected Piperazines, Morpholines, and Thiomorpholines from Aldehydes and SnAP Reagents

Commercially available SnAP (stannyl amine protocol) reagents allow the transformation of aldehydes and ketones into a variety of N-unprotected heterocycles. By identifying new ligands and reaction conditions, a robust catalytic variant that expands the substrate scope to previously inaccessible heteroaromatic substrates and new substitution patterns was realized. It also establishes the basis for a catalytic enantioselective process through the use of chiral ligands. SnAPcat! The identification of new ligands and reaction conditions provides a robust catalytic method for the synthesis of N-unprotected heterocycles using SnAP reagents. This catalytic variant expands the substrate scope to include previously inaccessible piperazines, morpholines, and thiomorpholines and establishes the basis for a catalytic enantioselective process through the use of chiral ligands.

1-(3-heterocyclyphenyl)-S-triazine-2,6,6-oxo or thiotrione herbicidal agents

There is provided a 1-(3-heterocyclylphenyl)-s-triazine-2, 4,6-oxo or thiotrione compound having the structural formula I STR1 Further provided are a composition and a method comprising that compound for the control of undesirable plant species.

1-(3-heterocyclylphenyl)-s-triazine-2,4,6-oxo or thiotrione herbicidal agents

There is provided a 1-(3-heterocyclylphenyl)-s-triazine-2,4,6-oxo or thiotrione compound having the structural formula I STR1 Further provided are a composition and a method comprising that compound for the control of undesirable plant species.