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

Description

1-(4'-Iodophenyl)butane is a clear yellow liquid that serves as an active pharmaceutical intermediate. It is also utilized in the synthesis and characterization of photoelectronic polymers containing the triphenylamine moiety, as well as in the palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides.

Uses

Used in Pharmaceutical Industry:
1-(4'-Iodophenyl)butane is used as an active pharmaceutical intermediate for the development and production of various pharmaceutical compounds.
Used in Photoelectronic Polymers Synthesis:
In the field of photoelectronics, 1-(4'-Iodophenyl)butane is used as a key component in the synthesis and characterization of polymers that contain the triphenylamine moiety, which is crucial for their electronic and optical properties.
Used in Chemical Synthesis:
1-(4'-Iodophenyl)butane is employed as a reagent in the palladium-catalyzed conversion process, where it aids in the transformation of aryl and vinyl triflates into bromides and chlorides, which are important intermediates in organic synthesis.

Upstream product

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

Downstream Products

• 1097205-84-9 2-((4-butylphenyl)ethynyl)-1,1'-biphenyl 
• 128839-62-3 (4-Butyl-phenyl)-fluoro-acetic acid ethyl ester 
• 1231745-26-8 3-(4-butylphenyl)pentane-2,4-dione 
• 1079397-65-1 C₆₂H₇₀ 
• 19165-51-6 1-butyl-4-(phenylethynyl)benzene 
• 104-51-8 1-butylbenzene 
• 15181-08-5 p-Ethyl-n-butylbenzene 
• 20651-71-2 4-butyl benzoic acid 
• 1173178-67-0 3-(4-butylphenyl)-4,5-diphenyl-4H-1,2,4-triazole 
• 61342-04-9 1-butyl-4-(trifluoromethyl)benzene 
• 1154051-48-5 dimethyl 4-(4-butylphenyl)cyclohexa-1,4-diene-1,2-dicarboxylate 
• 1154051-47-4 4-(4-n-butylphenyl)cyclohex-4-ene-1,1,2,2-tetracarbonitrile 
• 1154051-30-5 2-(p-n-butylphenyl)-1,3-butadiene 
• 916576-33-5 trans-4-n-butylcinnamic acid n-butyl ester 

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.

Synthesis, Solubility, and Reaction of Long Alkyl-Chained Hypervalent Iodine Benzyne Precursors

Long-chained hypervalent iodine benzyne precursors bearing ethyl, butyl, hexyl, octyl, decyl, dodecyl, and tetradecyl groups were synthesized, respectively. As the alkyl chain of the benzyne precursors is lengthened, the solubility in nonpolar organic solvents and the yield of the benzyne adduct with furan gradually increases.