99585-16-7

Basic information

• Product Name: 3-(2-CHLORO-PHENYLSULFANYL)-PROPIONIC ACID
• Synonyms: Propionicacid, 3-(o-chlorophenylthio)- (6CI);3-(2-Chlorophenylsulfanyl)propionic acid
• CAS NO: 99585-16-7
• Molecular Formula: C₉H₉ClO₂S
• Molecular Weight: 216.6846
• Mol File: 99585-16-7.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 356.7 °C at 760 mmHg
• Flash Point: 169.5 °C
• Appearance: /
• Density: 1.36 g/cm³
• Vapor Pressure: 1.05E-05mmHg at 25°C
• Refractive Index: 1.608
• CAS DataBase Reference: 3-(2-CHLORO-PHENYLSULFANYL)-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-CHLORO-PHENYLSULFANYL)-PROPIONIC ACID(99585-16-7)
• EPA Substance Registry System: 3-(2-CHLORO-PHENYLSULFANYL)-PROPIONIC ACID(99585-16-7)

Safety Data

• Hazardous Substances Data: 99585-16-7(Hazardous Substances Data)

Usage

General Description

3-(2-chloro-phenylsulfanyl)-propionic acid, also known as 2-Chloro-3-(phenylsulfanyl)propanoic acid, is a chemical compound with a molecular formula of C9H9ClO2S. It is a derivative of propanoic acid and contains a phenylsulfanyl group and a chlorine atom attached to the 2 and 3 positions, respectively. 3-(2-CHLORO-PHENYLSULFANYL)-PROPIONIC ACID is often used as a building block in the synthesis of pharmaceuticals and agrochemicals, and it exhibits anti-inflammatory and analgesic properties, making it potentially useful in the development of new medications for pain management and inflammation. Additionally, 3-(2-chloro-phenylsulfanyl)-propionic acid may also have applications in the field of organic synthesis and material science due to its unique chemical structure and reactivity.

InChI:InChI=1/C9H9ClO2S/c10-7-3-1-2-4-8(7)13-6-5-9(11)12/h1-4H,5-6H2,(H,11,12)

Upstream product

• 6320-03-2 2-chlorothiphenol 
• 79-10-7 acrylic acid 
• 590-92-1 3-Bromopropionic acid 
• 107-94-8 chloropropionic acid 
• 57-57-8 β-Propiolactone 

Downstream Products

• 1438433-29-4 (E)-8-chloro-2,3-dihydro-3-[(4-nitrophenylamino)methylene]-4H-1-benzothiopyran-4-one 
• 1438433-28-3 (E)-3-[(2-aminophenylamino)methylene]-8-chloro-2,3-dihydro-4H-1-benzothiopyran-4-one 
• 1438433-27-2 (E)-8-chloro-2,3-dihydro-3-[(phenylamino)methylene]-4H-1-benzothiopyran-4-one 
• 1421435-07-5 2-[2-(8-chlorothiochroman-4-ylidene)hydrazinyl]-5-phenylthiazole 
• 1315306-62-7 8'-chloro-3-(4-chlorophenyl)spiro[oxirane-2,3'-thiochroman]-4'-one 
• 60639-20-5 8-chloro-3,4-dihydro-2H-1-benzothiopyran-4-one 

Relevant articles and documents

Preparation method of halogenated benzothiazepine oxide, product prepared by preparation method and application of product

The invention discloses a preparation method of halogenated benzothiazepine oxide as well as a product prepared by the preparation method and application of the halogenated benzothiazepine oxide, andrelates to the technical field of chemical synthesis. Th

Synthesis of Novel Pterocarpen Analogues via [3?+?2] Coupling-Elimination Cascade of α,α-Dicyanoolefins with Quinone Monoimines

By employing triethylamine as a catalyst, [3?+?2] coupling-elimination cascade of α,α-dicyanoolefins with quinone monoimines was realized. The reactions afforded various novel pterocarpen analogues with generally moderate yields (up to 75%). In addition, a plausible reaction mechanism was proposed.

Ionic liquid catalyzed synthesis of 2-(indole-3-yl)-thiochroman-4-ones and their novel antifungal activities

2-(Indole-3-yl)-thiochroman-4-ones were synthesized via ionic liquid and tested for in vitro antifungal activity. The contribution of ionic liquid to Michael addition reaction is significant. Structures of all compounds are elucidated by 1H NMR, 13C NMR and HRMS. Most of these compounds showed better antifungal activity than fluconazole. The results suggest that 2-(indole-3-yl)-thiochroman-4-ones would be efficient antifungal agents.