36517-93-8

Basic information

• Product Name: 2-(propylthio)ethanamine(SALTDATA: HCl)
• Synonyms: 2-(propylthio)ethanamine(SALTDATA: HCl)
• CAS NO: 36517-93-8
• Molecular Formula: C₅H₁₃NS
• Molecular Weight: 155.68936
• Mol File: 36517-93-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(propylthio)ethanamine(SALTDATA: HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(propylthio)ethanamine(SALTDATA: HCl)(36517-93-8)
• EPA Substance Registry System: 2-(propylthio)ethanamine(SALTDATA: HCl)(36517-93-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 36517-93-8(Hazardous Substances Data)

Usage

General Description

2-(propylthio)ethanamine, also known as N-propylthioethanamine, is a chemical compound with the molecular formula C5H13NS. It is a member of the amine class of organic compounds and is commonly used in the synthesis of pharmaceuticals and other organic compounds. 2-(propylthio)ethanamine(SALTDATA: HCl) is typically found as a salt with hydrochloric acid, known as SALTDATA: HCl. It is a colorless liquid with a strong amine odor and is soluble in water and organic solvents. 2-(propylthio)ethanamine is known for its use as a building block in the production of various pharmaceuticals and is an important intermediate chemical in organic synthesis.

Upstream product

• 151-56-4 ethyleneimine 
• 107-03-9 1-thiopropane 
• 107-09-5 2-bromoethylamine 
• 926-39-6 sulfuric acid mono-(2-amino-ethyl ester) 
• 156-57-0 2-mercaptoethylamine hydrochloride 
• 106-94-5 propyl bromide 
• 870-24-6 2-chloroethanamine hydrochloride 

Downstream Products

• 1375005-56-3 C₁₁H₂₆NO₃PS 
• 682-30-4 Diethyl vinylphosphonate 
• 1005761-70-5 C₂₀H₂₃NOS 
• 1058113-09-9 (Z)-1,3-diphenyl-3-(2-(propylthio)ethylamino)prop-2-en-1-one 
• 1198786-81-0 (Z)-1-phenyl-3-(2-(propylthio)ethylamino)but-2-en-1-one 
• 1198786-85-4 (Z)-2-benzyl-1,3-diphenyl-3-(2-(propylthio)ethylamino)prop-2-en-1-one 
• 1198786-83-2 (Z)-3-(2-(propylthio)ethylamino)-1,3-di-p-tolylprop-2-en-1-one 
• 1198786-84-3 (Z)-1,3-bis(4-methoxyphenyl)-3-(2-(propylthio)ethylamino)prop-2-en-1-one 
• 1198786-86-5 (Z)-2-methyl-1,3-diphenyl-3-(2-(propylthio)ethylamino)prop-2-en-1-one 
• 71416-96-1 Cyclohex-1-ene-1,2-dicarboxylic acid 1-[(4-chloro-2-fluoro-phenyl)-amide] 2-[(2-propylsulfanyl-ethyl)-amide] 

Relevant articles and documents

Thermoresponsive Sulfone and Sulfoxide-Containing Polyacrylamides

A series of thermoresponsive polyacrylamides containing sulfide, sulfone, or sulfoxide was successfully prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization. The thermal properties of polyacrylamides with sulfone or sulfoxide, which have not been studied before, were investigated for the first time. While poly[N-(2-(propylsulfonyl)ethyl)acrylamide] (P2SO2) with sulfone groups was water insoluble, poly[N-(2-(propylsulfinyl)ethyl)acrylamide] (P2SO) with sulfoxide groups was water soluble, indicating that the sulfoxide moiety is more hydrophilic than sulfone. By controlling the end of the polymer chain, we synthesized poly[N-(2-(ethylsulfonyl)ethyl)acrylamide] (P1SO2) and poly[N-(2-(butylsulfinyl)ethyl)acrylamide] (P3SO), which exhibit an lower critical solution temperature (LCST) in water around 24–26°C. For adjusting a wide range of LCST, we synthesized the random copolymers by controlling the initial feed ratio of hydrophobic M2SO2 and hydrophilic M2SO. The amphiphilic block copolymers were also synthesized and assembled in water to yield the micelles. After adding H2O2 to this micellar solution, the hydrophobic block was oxidized and converted to a hydrophilic block, leading to the transformation of micelles to unimers.