500-41-4

Basic information

• Product Name: 3-FLUORODIPHENYLAMINE
• Synonyms: 3-FLUORODIPHENYLAMINE;3-FLUORODIPHENYLAMINE, 98% MIN.;3-Fluorodiphenylamine97%
• CAS NO: 500-41-4
• Molecular Formula: C₁₂H₁₀FN
• Molecular Weight: 187.21
• Product Categories: Fluorine series
• Mol File: 500-41-4.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 285.9 °C at 760 mmHg
• Flash Point: 126.7 °C
• Appearance: /
• Density: 1.172 g/cm³
• Vapor Pressure: 0.00272mmHg at 25°C
• Refractive Index: 1.613
• PKA: -0.12±0.30(Predicted)
• CAS DataBase Reference: 3-FLUORODIPHENYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-FLUORODIPHENYLAMINE(500-41-4)
• EPA Substance Registry System: 3-FLUORODIPHENYLAMINE(500-41-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 500-41-4(Hazardous Substances Data)

Usage

General Description

3-Fluorodiphenylamine is a chemical compound that belongs to the diphenylamine class of chemicals and contains a fluorine atom attached to a diphenylamine molecule. It is commonly used as an intermediate in organic synthesis and is primarily employed as a building block to create various pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 3-Fluorodiphenylamine is utilized as a research tool in the development of new compounds and has potential applications in the field of materials science and as a reagent in chemical reactions. This chemical is known for its stability and compatibility with a wide range of solvents, making it a versatile and valuable component in various industries.

InChI:InChI=1/C12H10FN/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9,14H

Upstream product

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Downstream Products

• 129622-62-4 3-fluorophenyl(phenyl)carbamic chloride 
• 1187856-50-3 2-(((1r,4r)-4-(((3-fluorophenyl)(phenyl)carbamoyloxy)methyl)cyclohexyl)methoxy)acetic acid 
• 1187857-73-3 tert-butyl 2-(((1r,4r)-4-(((3-fluorophenyl)(phenyl)carbamoyloxy)methyl)cyclohexyl)methoxy)acetate 
• 1187857-12-0 sodium 2-(((1r,4r)-4-(((3-fluorophenyl)(phenyl)carbamoyloxy)methyl)cyclohexyl)methoxy)acetate 
• 1187857-78-8 potassium 2-(((1r,4r)-4-(((3-fluorophenyl)(phenyl)carbamoyloxy)methyl)cyclohexyl)methoxy)acetate 
• 1217129-27-5 C₂₂H₂₈FN 
• 91505-71-4 1-(3-fluorophenyl)-2(1H,3H)-indolone 
• 1187857-72-2 ethyl 2-(((1R,4r)-4-(((3-fluorophenyl)(phenyl)carbamoyloxy)methyl)cyclohexyl)methoxy)acetate 
• 1187857-71-1 ((1r,4r)-4-(hydroxymethyl)cyclohexyl)methyl-3-fluorophenyl(phenyl)carbamate 
• 1187857-70-0 4-(dimethylamino)-1-((3-fluorophenyl)(phenyl)carbamoyl)pyridinium chloride 
• 91506-59-1 N-(3-fluorophenyl)-alpha-chloroacetanilide 

Relevant articles and documents

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

The present invention relates to a device for emitting light. Provided are a novel mixture capable of improving stability and longevity, an organic electronic element using the same, and an electronic device thereof. (by machine translation)

COMPOUND FOR ORGANIC ELECTRIC ELEMENT, ORGANIC ELECTRIC ELEMENT COMPRISING THE SAME AND ELECTRONIC DEVICE THEREOF

The present invention relates to a compound for allowing high luminous efficiency and low driving voltage in an element and increasing a lifespan thereof, and an organic electric element using the same, and an electronic device thereof. The compound is represented by chemical formula (1) in which Y is one of C and Si, and X^1 and X^2 are each independently the same or different, and are each selected from the group consisting of N-L^1-Ar^1, S and O.COPYRIGHT KIPO 2019

Reductive Molybdenum-Catalyzed Direct Amination of Boronic Acids with Nitro Compounds

The synthesis of aromatic amines is of utmost importance in a wide range of chemical contexts. We report a direct amination of boronic acids with nitro compounds to yield (hetero)aryl amines. The novel combination of a dioxomolybdenum(VI) catalyst and triphenylphosphine as inexpensive reductant has revealed to be decisive to achieve this new C?N coupling. Our methodology has proven to be scalable, air and moisture tolerant, highly chemoselective and engages both aliphatic and aromatic nitro compounds. Moreover, this general and step-economical synthesis of aromatic secondary amines showcases orthogonality to other aromatic amine syntheses as it tolerates aryl halides and carbonyl compounds.