25109-28-8

Basic information

• Product Name: 1-Bromo-4-cyclohexylbenzene
• Synonyms: 1-BROMO-4-CYCLOHEXYLBENZENE;4-BROMOPHENYLCYCLOHEXANE;4-Cyclohexylbromobenzene;p-bromophenylcyclohexane;4-Bromo-1-cyclohexylbenzene;Ai3-11173;Benzene, 1-bromo-4-cyclohexyl-;Einecs 246-623-3
• CAS NO: 25109-28-8
• Molecular Formula: C₁₂H₁₅Br
• Molecular Weight: 239.15
• EINECS: 246-623-3
• Mol File: 25109-28-8.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 90-94°C 0,01mm
• Flash Point: 90-94°C/0.01mm
• Appearance: /
• Density: 1,287 g/cm3
• Vapor Pressure: 0.00366mmHg at 25°C
• Refractive Index: 1.5595
• Storage Temp.: Sealed in dry,Room Temperature
• Water Solubility: Not miscible or difficult to mix with water.
• BRN: 2209869
• CAS DataBase Reference: 1-Bromo-4-cyclohexylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-4-cyclohexylbenzene(25109-28-8)
• EPA Substance Registry System: 1-Bromo-4-cyclohexylbenzene(25109-28-8)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 25109-28-8(Hazardous Substances Data)

Usage

Description

1-Bromo-4-cyclohexylbenzene is an organic compound characterized by its colorless to light yellow liquid appearance. It is a derivative of benzene with a bromine atom attached at the first position and a cyclohexyl group at the fourth position. 1-Bromo-4-cyclohexylbenzene is known for its unique chemical properties that make it suitable for various applications across different industries.

Uses

Used in Electronics Industry:
1-Bromo-4-cyclohexylbenzene is used as a material in the manufacturing of organic light-emitting diodes (OLEDs). Its chemical properties contribute to the efficient functioning of these devices, which are widely used in display technologies and lighting applications due to their high energy efficiency, thin and lightweight design, and fast response times.
Used in Pharmaceutical Industry:
1-Bromo-4-cyclohexylbenzene serves as a valuable intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for further chemical modifications, making it a versatile building block in the development of new drugs. The compound's role in the pharmaceutical industry highlights its importance in the creation of novel therapeutic agents that can address a range of health concerns.

InChI:InChI=1/C12H15Br/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h6-10H,1-5H2

Upstream product

• 108-86-1 bromobenzene 
• 110-83-8 cyclohexene 
• 827-52-1 1-phenyl-1-cyclohexane 
• 108-85-0 1-bromocyclohexane 
• 5467-74-3 4-Bromophenylboronic acid 
• 108-91-8 cyclohexylamine 
• 589-87-7 1,4-bromoiodobenzene 
• 931-51-1 cyclohexylmagnesiumchloride 
• 98-89-5 Cyclohexanecarboxylic acid 
• 52939-54-5 4-cyclohexylhepta-1,6-dien-4-ol 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 108-93-0 cyclohexanol 
• 110-82-7 cyclohexane 
• 1605-17-0 1-Bromo-4-(1-cyclohexen-1-yl)benzene 

Downstream Products

• 57803-90-4 3-(4-Cyclohexyl-phenyl)-1H-indene 
• 6728-90-1 3-(p-Cyclohexyl-phenyl)-2-hydroxy-propylchlorid 
• 87-82-1 hexabromobenzene 
• 861097-00-9 Hydroxy-phenyl-bis-(4-cyclohexyl-phenyl)-methan 
• 872793-68-5 Hydroxy-tris-(4-cyclohexyl-phenyl)-methan 
• 820223-94-7 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl))phenylcyclohexane 
• 57263-22-6 1-(4-cyclohexyl-phenyl)-2,2,4,4-tetramethyl-3-(4-pyridin-2-yl-piperazin-1-yl)-cyclobutanol 
• 1535207-51-2 ((4-cyclohexylphenyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl)trimethylsilane 
• 1467059-08-0 6-chloro-5-(4-cyclohexylphenyl)-1H-indazole-3-carboxylic acid 
• 1421703-76-5 C₃₀H₃₉Cl₂N₅O 
• 1417306-57-0 (4-cyclohexylphenyl)phosphonic acid 
• 1417306-54-7 diethyl (4-cyclohexylphenyl)phosphonate 
• 1391920-75-4 (R)-3-(4-cyclohexylphenyl)cycloheptanone 
• 1337917-06-2 2-(4-cyclohexylphenyl)-2H-1,2,3-triazole 

Relevant articles and documents

Organic compound and, electronic component using same, and electronic device

The invention belongs to the field of organic materials, and relates to an organic compound and and an electronic device using the same, wherein the organic compound has the structure shown in Chemical Formula 1, the organic compound is applied to an organic electroluminescent device, and the performance of the device can be remarkably improved.

Ni-catalyzed Reductive Deaminative Arylation at sp3 Carbon Centers

A Ni-catalyzed reductive deaminative arylation at unactivated sp3 carbon centers is described. This operationally simple and user-friendly protocol exhibits excellent chemoselectivity profile and broad substrate scope, thus complementing existing metal-catalyzed cross-coupling reactions to forge sp3 C-C linkages. These virtues have been assessed in the context of late-stage functionalization, hence providing a strategic advantage to reliably generate structure diversity with amine-containing drugs.

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids

A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross-coupling between alkyl-carboxylic acids and boronic acids is described. This Ni-catalyzed reaction relies upon the activation of alkyl carboxylic acids as their redox-active ester derivatives, specifically N-hydroxy-tetrachlorophthalimide (TCNHPI), and proceeds in a practical and scalable fashion. The inexpensive nature of the reaction components (NiCl2?6 H2O—$9.5 mol?1, Et3N) coupled to the virtually unlimited commercial catalog of available starting materials bodes well for its rapid adoption.