68104-61-0

Basic information

• Product Name: 1-(4-TERT-BUTYLPHENYL)PIPERAZINE
• Synonyms: 1-(4-TERT-BUTYLPHENYL)PIPERAZINE
• CAS NO: 68104-61-0
• Molecular Formula: C₁₄H₂₂N₂
• Molecular Weight: 218.34
• EINECS: 268-473-8
• Mol File: 68104-61-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 346.4°Cat760mmHg
• Flash Point: 140.7°C
• Appearance: /
• Density: 0.972g/cm³
• Vapor Pressure: 5.79E-05mmHg at 25°C
• Refractive Index: 1.519
• CAS DataBase Reference: 1-(4-TERT-BUTYLPHENYL)PIPERAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-TERT-BUTYLPHENYL)PIPERAZINE(68104-61-0)
• EPA Substance Registry System: 1-(4-TERT-BUTYLPHENYL)PIPERAZINE(68104-61-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 68104-61-0(Hazardous Substances Data)

Usage

General Description

1-(4-tert-butylphenyl)piperazine is a chemical compound with a molecular formula C16H24N2. It is a piperazine derivative with a substituted phenyl ring, and the tert-butyl group attached to the phenyl ring. This chemical has been studied for its potential pharmacological properties, such as its use in the development of drugs for various medical conditions. It is also used as a building block in the synthesis of other organic compounds. Despite its potential applications, further research is needed to fully understand its biological and chemical properties.

InChI:InChI=1/C14H22N2/c1-14(2,3)12-4-6-13(7-5-12)16-10-8-15-9-11-16/h4-7,15H,8-11H2,1-3H3

Upstream product

• 769-92-6 4-tert-Butylaniline 
• 821-48-7 bis-(2-chloroethyl)amine hydrochloride 
• 110-85-0 piperazine 
• 3972-65-4 1-bromo-4-tert-butylbenzene 

Downstream Products

• 1204976-74-8 C₂₇H₃₃FN₄ 
• 1239717-01-1 1-((1H-imidazol-4-yl)methyl)-4-(4-tert-butylphenyl)-piperazine 
• 1247040-90-9 C₁₈H₂₈N₂O₂ 

Relevant articles and documents

(DiMeIHeptCl)Pd: A Low-Load Catalyst for Solvent-Free (Melt) Amination

(DiMeIHeptCl)Pd, a hyper-branched N-aryl Pd NHC catalyst, has been shown to be efficient at performing amine arylation reactions in solvent-free ("melt") conditions. The highly lipophilic environment of the alkyl chains flanking the Pd center serves as lubricant to allow the complex to navigate through the paste-like environment of these mixtures. The protocol can be used on a multi-gram scale to make a variety of aniline derivatives, including substrates containing alcohol moieties.

NOVEL 1,6-DISUBSTITUTED-3-AMINO-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE COMPOUNDS AND PREPARATION THEREOF

Provided are a novel 1,6-disubstituted-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one compound, a pharmaceutically acceptable salt compound thereof, a method for preparing the compound, and an anticancer pharmaceutical composition including the compound as an effective ingredient.