887625-49-2

Basic information

• Product Name: 2,4-DIFLUOROPHENACYL THIOCYANATE
• Synonyms: 2,4-DIFLUOROPHENACYL THIOCYANATE;2-(cyanosulfanyl)-1-(2,4-difluorophenyl)ethan-1-one
• CAS NO: 887625-49-2
• Molecular Formula: C₉H₅F₂NOS
• Molecular Weight: 213.2
• Mol File: 887625-49-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 338.9°C at 760 mmHg
• Flash Point: 158.7°C
• Appearance: /
• Density: 1.391g/cm³
• Vapor Pressure: 9.54E-05mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: 2,4-DIFLUOROPHENACYL THIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIFLUOROPHENACYL THIOCYANATE(887625-49-2)
• EPA Substance Registry System: 2,4-DIFLUOROPHENACYL THIOCYANATE(887625-49-2)

Safety Data

• Hazardous Substances Data: 887625-49-2(Hazardous Substances Data)

Usage

General Description

2,4-Difluorophenacyl thiocyanate is a chemical compound that is derived from the thiocyanate salt of 2,4-difluorophenacyl alcohol. It is commonly used as a pesticide and insecticide for agricultural purposes. The compound works by disrupting the pest's nervous system and inhibiting its ability to feed and reproduce. It is also effective against a wide range of pests and is generally considered to have low toxicity to mammals and other non-target organisms when used properly. However, it is important to handle and use this chemical with caution, following proper safety protocols and guidelines to minimize the risk of harm to humans and the environment.

InChI:InChI=1/C9H5F2NOS/c10-6-1-2-7(8(11)3-6)9(13)4-14-5-12/h1-3H,4H2

Upstream product

• 399-53-1 2,4-difluorobenzaldehyde 
• 1147550-11-5 ammonium thiocyanate 
• 102429-07-2 2-bromo-2',4'-difluoroacetophenone 
• 333-20-0 potassium thioacyanate 

Downstream Products

• 887625-52-7 4-(2,4-difluorophenyl)-2-(piperazin-1-yl)thiazole 
• 887623-58-7 4-(4-(2,4-difluorophenyl)thiazol-2-yl)-N-(3,4-dimethylisoxazol-5-yl)piperazine-1-carboxamide 
• 887625-50-5 2-bromo-4-(2,4-difluorophenyl)thiazole 
• 887625-51-6 tert-butyl 4-[4-(2,4-difluorophenyl)thiazol-2-yl]piperazine-1-carboxylate 

Relevant articles and documents

A 2-thiocyano HYPNONE derivatives method for the preparation of

The invention discloses a method for preparing 2-sulfur cyano acetophenone derivatives. The method for preparing the 2-sulfur cyano acetophenone derivatives comprises the following steps: dissolving styrene derivatives and ammonium thiocyanate in a solvent, and reacting at 20-30 DEG C to obtain 2-sulfur cyano acetophenone derivatives. According to the method for preparing the 2-sulfur cyano acetophenone derivatives, the styrene derivatives are taken as starting materials; the raw materials are easily available and various in type; products prepared by the method have various in type, can be directly used and can also be used for other further reactions; meanwhile, the method is mild in reaction conditions and simple in reaction operation and post-processing process; an accelerant does not need to be added; the production process meets the green and chemical requirements, is relatively high in yield and is suitable for large-scale production.