91552-82-8

Basic information

• Product Name: 2-(4-TERT-BUTYLPHENYL)ETHYLAMINE
• Synonyms: RARECHEM AL BW 0742;2-(4-TERT-BUTYLPHENYL)ETHYALMINE;2-(4-TERT-BUTYLPHENYL)ETHYLAMINE;4-(TERT-BUTYL)PHENETHYLAMINE;Butylphenylethylamine;2-(4-tert-Butylphenyl)ethylamine 97%
• CAS NO: 91552-82-8
• Molecular Formula: C₁₂H₁₉N
• Molecular Weight: 177.29
• Mol File: 91552-82-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 80 °C
• Flash Point: 115.7 °C
• Appearance: /
• Density: 0.92g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(4-TERT-BUTYLPHENYL)ETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-TERT-BUTYLPHENYL)ETHYLAMINE(91552-82-8)
• EPA Substance Registry System: 2-(4-TERT-BUTYLPHENYL)ETHYLAMINE(91552-82-8)

Safety Data

• Hazard Codes: Xi
• Statements: 34
• Safety Statements: 26-36/37/39
• RIDADR: 2735
• Hazardous Substances Data: 91552-82-8(Hazardous Substances Data)

Usage

General Description

2-(4-tert-butylphenyl)ethylamine is a chemical compound with the molecular formula C14H23N. It is a secondary amine, which means it contains a nitrogen atom bonded to two carbon atoms. 2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is a colorless liquid at room temperature, and it is commonly used as a raw material in the production of various pharmaceuticals and organic compounds. Its structure includes a tert-butyl group, which contributes to its stability and resistance to oxidation. 2-(4-tert-butylphenyl)ethylamine has been studied for its potential use as a building block in organic synthesis and drug development, and it is also used in research and development applications.

Upstream product

• 3288-99-1 4-tert-butylbenzyl cyanide 
• 100368-57-8 2-(4-(tert-butyl)phenyl)acetamide 
• 3549-23-3 methyl 2-(4-tert-butylphenyl)acetate 
• 32857-63-9 4-t-butylphenylacetic acid 
• 1746-23-2 4-tert-Butylstyrene 

Downstream Products

• 184003-55-2 1-tert-butyl-4-(2-isothiocyanatoethyl)benzene 
• 184003-56-3 1-[2-(4-tert-Butyl-phenyl)-ethyl]-3-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethoxy]-3-methoxy-benzyl}-thiourea 
• 274914-89-5 3-[2-(4-tert-Butyl-phenyl)-ethylamino]-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dione 
• 134531-77-4 N-[2-[4-(t-butyl)phenyl]ethyl]-1,5-naphthyridin-4-amine 
• 134999-96-5 4-[2-[4-(t-butyl)phenyl]ethylamino]pyrido-[4,3-d]pyrimidine 
• 1067904-10-2 C₂₀H₂₄N₂O₃S 

Relevant articles and documents

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

Biarylpropylsulfonamides as novel, potent potentiators of 2-amino-3-(5-methyl-3-hydroxyisoxazol-4-yl)-propanoic acid (AMPA) receptors [1]

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