17078-76-1

Basic information

• Product Name: 4-ETHYL-4'-IODOBIPHENYL
• Synonyms: 4-ETHYL-4'-IODOBIPHENYL;4-Ethyl-4'-iodobiphenyl;4-iodo-4'-ethylbiphenyl;HYL-4'-IODOBIPHENYL
• CAS NO: 17078-76-1
• Molecular Formula: C₁₄H₁₃I
• Molecular Weight: 308.16
• Product Categories: Biphenyl & Diphenyl ether
• Mol File: 17078-76-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 347.4 °C at 760 mmHg
• Flash Point: 157.5 °C
• Appearance: /
• Density: 1.47 g/cm³
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-ETHYL-4'-IODOBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ETHYL-4'-IODOBIPHENYL(17078-76-1)
• EPA Substance Registry System: 4-ETHYL-4'-IODOBIPHENYL(17078-76-1)

Safety Data

• Hazardous Substances Data: 17078-76-1(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 5707-44-8 4-ethylbiphenyl 
• 10450-60-9 periodic acid 
• 624-38-4 para-diiodobenzene 
• 25309-64-2 4-ethyl-1-iodobenzene 
• 58743-79-6 1-bromo-4-(4'-ethylphenyl)benzene 
• 5467-74-3 4-Bromophenylboronic acid 
• 1591-31-7 4-iodo-biphenyl 
• 5731-02-2 4-Acetyl-4'-iodobiphenyl 

Downstream Products

• 179063-49-1 N,N'-bis(4-methylphenyl)-N,N'-bis(4'-ethylbiphenyl-4-yl)-1,3-naphthylenediamine 
• 167377-26-6 N,N'-di-p-tolyl-N,N'-di(4'-ethylbiphenyl-4-yl)-3,3'-dimethylbenzidine 

Relevant articles and documents

The Multiple Facets of Iodine(III) Compounds in an Unprecedented Catalytic Auto-amination for Chiral Amine Synthesis

Iodine(III) reagents are used in catalytic one-pot reactions, first as both oxidants and substrates, then as cross-coupling partners, to afford chiral polyfunctionalized amines. The strategy relies on an initial catalytic auto C(sp3)?H amination of the iodine(III) oxidant, which delivers an amine-derived iodine(I) product that is subsequently used in palladium-catalyzed cross-couplings to afford a variety of useful building blocks with high yields and excellent stereoselectivities. This study demonstrates the concept of self-amination of the hypervalent iodine reagents, which increases the value of the aryl moiety.

Novel fluorescent carbazole derivative

The object of this invention is to provide an illuminant, which can easily be produced at low cost. This invention is a carbazole derivative luminescent compound having a carbazole ring skeleton, to the nitrogen atom of which is attached an electron-donat