28824-66-0

Basic information

• Product Name: AKOS B018368
• Synonyms: ART-CHEM-BB B018368;CHEMBRDG-BB 3018368;AKOS B018368;(5E)-5-(1,3-benzodioxol-5-ylmethylene)-2-mercapto-1,3-thiazol-4(5H)-one;Nsc31059;(5E)-5-(1,3-benzodioxol-5-ylmethylene)-2-mercapto-1,3-thiazol-4(5H)-one(SALTDATA: FREE);(5E)-5-(1,3-Benzodioxol-5-ylmethylene)-2-thioxo-1,3-thiazolidin-4-one;(5E)-5-(1,3-benzodioxol-5-ylmethylene)-2-thioxo-4-thiazolidinone
• CAS NO: 28824-66-0
• Molecular Formula: C₁₁H₇NO₃S₂
• Molecular Weight: 265.31
• Mol File: 28824-66-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.62g/cm³
• Vapor Pressure: 1.81E-07mmHg at 25°C
• Refractive Index: 1.768
• Storage Temp.: 2-8°C
• CAS DataBase Reference: AKOS B018368(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS B018368(28824-66-0)
• EPA Substance Registry System: AKOS B018368(28824-66-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 28824-66-0(Hazardous Substances Data)

Usage

General Description

AKOS B018368, also known as 3-Amino-1-propanesulfonic acid, is a chemical compound with the molecular formula C3H9NO3S. It is a colorless, water-soluble solid commonly used as a chelating agent and as a raw material in the synthesis of pharmaceuticals. AKOS B018368 has various industrial applications, including in the production of metal ion complexing agents and as a component in detergents and cleaning products. It is also used in the manufacture of water treatment chemicals and pharmaceutical intermediates. Additionally, AKOS B018368 has potential applications in the agricultural industry as a plant growth regulator. Overall, this compound has a wide range of uses in various industries due to its chelating and complexing properties.

InChI:InChI=1/C11H7NO3S2/c13-10-9(17-11(16)12-10)4-6-1-2-7-8(3-6)15-5-14-7/h1-4H,5H2,(H,12,13,16)/b9-4+

Upstream product

• 120-57-0 piperonal 
• 4303-27-9 2,4-dithioxothiazolidine 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 141-84-4 2-thioxo-4-thiazolidinone 
• 111-42-2 2,2'-iminobis[ethanol] 

Downstream Products

• 1415582-59-0 C₂₉H₃₀N₆O₅S₂ 
• 843641-27-0 5-[(benzo[d][1,3]dioxol-6-yl)methylene]-2-(benzylamino)thiazol-4(5H)-one 
• 55111-60-9 5-[(benzo[d][1,3]dioxol-6-yl)methylene]-2-(piperidin-1-yl)thiazol-4(5H)-one 
• 65562-22-3 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(tetra-O-acetyl-β-D-glucopyranosyl)-2-thioxo-thiazolidin-4-one 
• 68142-57-4 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2,4-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-58-5 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-68-7 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(3-chloro-2-methyl-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-67-6 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(6-chloro-3-methyl-2,4-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-66-5 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2,3-dichloro-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-64-3 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2-methyl-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-60-9 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2-chloro-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-65-4 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(4-methyl-2,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-61-0 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(2-bromo-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 
• 68142-63-2 5-(Z)-benzo[1,3]dioxol-5-ylmethylene-3-(4-chloro-2,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one 

Relevant articles and documents

Design and microwave synthesis of new (5z) 5-arylidene-2-thioxo-1,3-thiazolinidin-4-one and (5z) 2-amino-5-arylidene-1,3-thiazol-4(5h)-one as new inhibitors of protein kinase dyrk1a

Here, we report on the synthesis of libraries of new 5-arylidene-2-thioxo-1,3-thiazolidin-4-ones 3 (twenty-two compounds) and new 2-amino-5-arylidene-1,3-thiazol-4(5H)-ones 5 (twenty-four compounds) with stereo controlled Z-geometry under microwave irradi

Uses of 2-(thiophene-2-carbonylcarbamothioylthio)acetic acid as a good synthon for construction of some new thiazole and annulated thiazole derivatives

The reaction of thiophene-2-carbonyl isothiocyanate 2 with thioglycolic acid gave 2-(thiophene-2-carbonylcarbamothioylthio) acetic acid 3. Compound 3 was subjected to some selected reactions with sulphuric acid as well as benzaldehyde, piperonal and isati

Microwave-Assisted condensation reactions of acetophenone derivatives and activated methylene compounds with aldehydes catalyzed by boric acid under solvent-free conditions

We here disclosed a new protocol for the condensation of acetophenone derivatives and active methylene compounds with aldehydes in the presence of boric acid under microwave conditions. Implementation of the reaction is simple, healthy and environmentally