2-(4-tert-Butylphenyl)ethylamine

Base Information

• Chemical Name: 2-(4-tert-Butylphenyl)ethylamine
• CAS No.: 91552-82-8
• Molecular Formula: C12H19N
• Molecular Weight: 177.29
• Hs Code.: 2921499090
• European Community (EC) Number: 671-024-2
• DSSTox Substance ID: DTXSID50370886
• Nikkaji Number: J1.046.835C
• Wikidata: Q82158053
• ChEMBL ID: CHEMBL474882
• Mol file: 91552-82-8.mol

Synonyms:91552-82-8;2-(4-tert-Butylphenyl)ethylamine;2-(4-(tert-Butyl)phenyl)ethanamine;2-(4-tert-butylphenyl)ethanamine;2-(4-tert-butylphenyl)ethyalmine;2-(4-tert-butylphenyl)ethan-1-amine;CHEMBL474882;4-(tert-butyl)phenethylamine;Benzeneethanamine, 4-(1,1-dimethylethyl)-;SODIUMPYROVANADATE;4-tert-Butylphenethylamine;4-tert-butyl-phenethylamine;2-(4-t-Buphenyl)ethylamine;SCHEMBL716077;DTXSID50370886;WKCZSFRAGKIIKN-UHFFFAOYSA-N;2-[4-(t-butyl)phenyl]ethylamine;N-(4-tert-butylbenzyl)methylamine;2-(4-tert-Butyl-phenyl)-ethylamine;BDBM50262760;MFCD00082596;AKOS000163315;N-[2-[4-(t-butyl)phenyl]ethyl]amine;AS-44246;Benzeneethanamine,4-(1,1-dimethylethyl)-;FT-0642205;EN300-39256;A843977;Z285143726

Chemical Property of 2-(4-tert-Butylphenyl)ethylamine

Chemical Property:

• Boiling Point: 259.3 °C at 760 mmHg
• Flash Point: 115.7 °C
• PSA: 26.02000
• Density: 0.92g/cm³
• LogP: 3.18560
• Storage Temp.: 2-8°C
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 177.151749610
• Heavy Atom Count: 13
• Complexity: 138

Purity/Quality:

99% ^*data from raw suppliers

2-(4-(tert-butyl)phenyl)ethanamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 34
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)C1=CC=C(C=C1)CCN

Technology Process of 2-(4-tert-Butylphenyl)ethylamine

There total 5 articles about 2-(4-tert-Butylphenyl)ethylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

4-tert-Butylstyrene (1746-23-2,26009-55-2) → N-[2-[4-(t-butyl)phenyl]ethyl]amine (91552-82-8)

Guidance literature:

With 10-phenyl-9-(2,4,6-trimethylphenyl)acridinium tetrafluoroborate; ammonium carbonate; 2-amino-benzenethiol; In dichloromethane; chlorobenzene; at 20 ℃; for 12h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation;

DOI:10.1002/anie.202016679

Reference yield:

4-tert-butylbenzyl cyanide (3288-99-1) → N-[2-[4-(t-butyl)phenyl]ethyl]amine (91552-82-8)

Guidance literature:

With lithium aluminium tetrahydride; diethyl ether;

DOI:10.1021/jo01106a047

Reference yield:

2-(4-(tert-butyl)phenyl)acetamide (100368-57-8) → N-[2-[4-(t-butyl)phenyl]ethyl]amine (91552-82-8)

Guidance literature:

With borane-THF; In tetrahydrofuran; at 20 ℃;

DOI:10.1021/jm0002836

upstream raw materials:

4-tert-butylbenzyl cyanide

2-(4-(tert-butyl)phenyl)acetamide

methyl 2-(4-tert-butylphenyl)acetate

4-t-butylphenylacetic acid

Refernces

• 1、 -. "PROCESS FOR PRODUCING DIHYDROISOQUINOLINE ZWITTERIONS". Page/Page column 16. . Retrieved 2008/06/13.