20651-67-6

Basic information

• Product Name: 1-(4'-IODOPHENYL)BUTANE
• Synonyms: P-BUTYLIODOBENZENE;4-N-BUTYLIODOBENZENE;1-N-BUTYL-4-IODOBENZENE;1-(4'-IODOPHENYL)BUTANE;1-BUTYL-4-IODOBENZENE;4-Iodo-n-butylbenzene;1-Iodo-4-butylbenzene;4-Butyl-1-iodobenzene
• CAS NO: 20651-67-6
• Molecular Formula: C₁₀H₁₃I
• Molecular Weight: 260.11
• Product Categories: Iodine Compounds
• Mol File: 20651-67-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 80-82°C 0,5mm
• Flash Point: 80-82°C/0.5mm
• Appearance: clear yellow liquid
• Density: 1,462 g/cm3
• Refractive Index: 1.5690
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Water Solubility: Sparingly soluble in water at 25°C 3.6E-3 g/L.
• Sensitive: Light Sensitive
• BRN: 3030029
• CAS DataBase Reference: 1-(4'-IODOPHENYL)BUTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4'-IODOPHENYL)BUTANE(20651-67-6)
• EPA Substance Registry System: 1-(4'-IODOPHENYL)BUTANE(20651-67-6)

Safety Data

• Hazardous Substances Data: 20651-67-6(Hazardous Substances Data)

Usage

Chemical Properties

clear yellow liquid

Uses

It is used as an active pharmaceutical intermediate. It is also used in the synthesis and characterization of photoelectronic polymers containing triphenylamine moiety and in the palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.

Upstream product

• 104-51-8 1-butylbenzene 
• 7553-56-2 iodine 
• 7782-68-5 iodic acid 
• 64-19-7 acetic acid 
• 77153-60-7 1-(4-Butylphenyl)-3,3-(1,5-pentanediyl)triazene 
• 109-72-8 n-butyllithium 
• 624-38-4 para-diiodobenzene 
• 110-00-9 furan 
• 104-13-2 4-Butylaniline 
• 41492-05-1 p-bromobutylbenzene 

Downstream Products

• 434-90-2 decafluorobiphenyl 
• 131894-75-2 4'-butyl-2,3,4,5,6-pentafluoro-1,1'-biphenyl 
• 167864-23-5 4,N-dibutyl-aniline 
• 78888-05-8 N-(4-n-butylphenyl)benzenamine 
• 65717-69-3 (4-n-butylphenyl)diphenylphosphine 
• 1173178-67-0 3-(4-butylphenyl)-4,5-diphenyl-4H-1,2,4-triazole 
• 104-51-8 1-butylbenzene 
• 15181-08-5 p-Ethyl-n-butylbenzene 
• 20651-71-2 4-butyl benzoic acid 
• 1231745-26-8 3-(4-butylphenyl)pentane-2,4-dione 
• 61342-04-9 1-butyl-4-(trifluoromethyl)benzene 
• 1366392-18-8 1-butyl-4-(difluoromethyl)benzene 
• 1469444-96-9 (Z)-1-butyl-4-(2-phenyl-2-p-butylphenylvinyl)benzene 
• 1469445-26-8 (E)-1-butyl-4-(2-phenyl-2-p-butylphenylvinyl)benzene 

Relevant articles and documents

Halogen-bonded liquid crystals of 4-alkoxystilbazoles with molecular iodine: A very short halogen bond and unusual mesophase stability

Complexes of molecular iodine with alkoxystilbazoles are liquid crystals with unusually high mesophase stability, predicated on an intermolecular I...I contact. Attempts to prepare analogous complexes with bromine led to an unexpected electrophilic substitution product.

Tunable luminescence of new photochromic bisthienylethenes containing triphenylamine

Two new photochromic 1,2-bisthienylethenes containing triphenylamine were conveniently prepared; large cyclization quantum yields and obvious fluorescent changes regulated by the photoisomerization were observed. The substitution effect on the photochromic process is discussed based on these systems. CSIRO 2005.

Tetraorganoindates as Nucleophilic Coupling Partners in Pd-Catalyzed Cross-Coupling Reactions

(Equation presented) In situ generated ate complex In situ-generated tetraorganoindate complexes from the reaction of 1 equiv of indium trichloride with 4 equiv of appropriate organometallics are efficient nucleophiles in Pd-catalyzed cross-coupling reactions. In this novel reaction tetraorganoindates containing methyl, 1°- and 2°-alkyl, vinyl, alkynyl, and aryl groups transfer the four organic groups to a variety of electrophiles with high atom efficiency.