37920-25-5

Basic information

• Product Name: 1-(4-Butylphenyl)ethan-1-one
• Synonyms: 1-(4-butylphenyl)-ethanon;Ethanone, 1-(4-butylphenyl)-;P-BUTYLACETOPHENONE;LABOTEST-BB LT00159031;1-(4-BUTYL-PHENYL)ETHANONE;1-(4-BUTYLPHENYL)ETHAN-1-ONE;4'-N-BUTYLACETOPHENONE;4-N-BUTYLACETOPHENONE
• CAS NO: 37920-25-5
• Molecular Formula: C₁₂H₁₆O
• Molecular Weight: 176.25
• EINECS: 253-715-7
• Product Categories: Aromatic Acetophenones & Derivatives (substituted);Phenyls & Phenyl-Het;Acetophenones (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials;Phenyls & Phenyl-Het;C11 to C12;Carbonyl Compounds;Ketones;Building Blocks;C11 to C12;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 37920-25-5.mol
• Article Data: 61

Chemical Properties

• Boiling Point: 101-102 °C1.5 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: Clear colorless to pale yellow/Liquid
• Density: 0.957 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00522mmHg at 25°C
• Refractive Index: 1.5170-1.5220
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform, Ethyl Acetate (Slightly)
• Water Solubility: Not miscible in water.
• CAS DataBase Reference: 1-(4-Butylphenyl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Butylphenyl)ethan-1-one(37920-25-5)
• EPA Substance Registry System: 1-(4-Butylphenyl)ethan-1-one(37920-25-5)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 22-36/37/38
• Safety Statements: 23-26-36/37/39
• WGK Germany: 3
• TSCA: Yes
• HazardClass: IRRITANT
• Hazardous Substances Data: 37920-25-5(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 37920-25-5 differently. You can refer to the following data:
1. Intermediates of Liquid Crystals
2. 4'-n-Butylacetophenone is used as an organic chemical synthesis intermediate.

InChI:InChI=1/C12H16O/c1-3-4-5-11-6-8-12(9-7-11)10(2)13/h6-9H,3-5H2,1-2H3

Upstream product

• 1571-86-4 1,4-dibutyl-benzene 
• 104-51-8 1-butylbenzene 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 123-86-4 acetic acid butyl ester 
• 71-43-2 benzene 
• 960-16-7 tributylphenylstannane 
• 109613-00-5 4-acetophenyl triflate 
• 1461-25-2 tetra-n-butyltin(IV) 
• 109-72-8 n-butyllithium 
• 98-86-2 acetophenone 
• 6638-68-2 4,5-dimethyl-2-phenyl-1,3,2-dioxaborolane 
• 69497-83-2 4-acetylphenyl mesylate 
• 7446-70-0 aluminium trichloride 

Downstream Products

• 91552-69-1 α-<4-Butyl-phenyl>-aethylamin 
• 183670-22-6 2-(p-butylphenyl)quinoline-4-carboxylic acid 
• 100-21-0 terephthalic acid 
• 20651-71-2 4-butyl benzoic acid 
• 852815-58-8 ethyl 4-(4-butylphenyl)-2,4-dioxobutanoate 
• 1359983-79-1 C₁₈H₂₅N₃O₂ 
• 1359983-61-1 4-(4-butylphenyl)-1H-imidazol-2-amine hydrochloride 
• 1212171-18-0 C₁₂H₁₉N 
• 1212107-18-0 C₁₂H₁₉N 
• 1430109-89-9 (E)-1-(4-butylphenyl)-4-(4-methoxyphenyl)but-2-ene-1,4-dione 
• 1430109-96-8 (Z)-1-(4-butylphenyl)-4-(4-methoxyphenyl)but-2-ene-1,4-dione 
• 1430109-91-3 (E)-1-(4-butylphenyl)-4-(4-fluorophenyl)but-2-ene-1,4-dione 
• 102158-72-5 (E)-1-(4-butylphenyl)-4-phenylbut-2-ene-1,4-dione 
• 64128-27-4 1-(4-butyl-phenyl)-ethanone oxime 

Relevant articles and documents

Unprecedented nucleophilic addition of organolithiums to aromatic aldehydes and ketones by complexation with aluminum tris(2,6-diphenylphenoxide)

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Design of Benzimidazolyl Phosphines Bearing AlterableP,OorP,N-Coordination: Synthesis, Characterization, and Insights into Their Reactivity

A new series of hemilabile benzimidazolyl phosphines is reported. Entities in this ligand family can be easily assembled and prepared on a large scale via a simple one-pot procedure. X-ray crystallographic analyses show that the Pd metal center can coordinate in different fashions, where it relies on the size of the ?PR2group. With the same ligand scaffold, the ligand having a ?PCy2moiety displays better efficiency in expediting aromatic C-C bond-coupling reactions, while the ligand associated with a ?P-t-Bu2group, in contrast, promotes C-N bond-forming reactions.

Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate

The generation of tertiary, secondary, and primary alkyl radicals has been achieved by the direct visible-light excitation of a boracene-based alkylborate. This system is based on the photophysical properties of the organoboron molecule. The protocol is applicable to decyanoalkylation, Giese addition, and nickel-catalyzed carbon-carbon bond formations such as alkyl-aryl cross-coupling or vicinal alkylarylation of alkenes, enabling the introduction of various C(sp3) fragments to organic molecules.