| Identification | More | [Name]
2-tert-Butylaniline | [CAS]
6310-21-0 | [Synonyms]
2-TERT-BUTYLANILINE
AKOS BBS-00003572
Aniline, 2-tert-butyl-
2-TERT-BUTYLPHENYLAMINE
2-(1,1-Dimethylethyl)benzenamine
2-tert-Butylbenzenamine | [EINECS(EC#)]
228-634-5 | [Molecular Formula]
C10H15N | [MDL Number]
MFCD00130023 | [Molecular Weight]
149.23 | [MOL File]
6310-21-0.mol |
| Chemical Properties | Back Directory | [Appearance]
clear pale yellow to red-brown liquid | [Melting point ]
-60 °C (lit.) | [Boiling point ]
123-124 °C/17 mmHg (lit.) | [density ]
0.957 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.545(lit.)
| [Fp ]
216 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Liquid | [pka]
3.78±0.10(Predicted) | [color ]
Clear pale yellow to red-brown | [InChIKey]
AEIOZWYBDBVCGW-UHFFFAOYSA-N | [CAS DataBase Reference]
6310-21-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzenamine, 2-(1,1-dimethylethyl)-(6310-21-0) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29214990 |
| Hazard Information | Back Directory | [Chemical Properties]
clear pale yellow to red-brown liquid | [Uses]
2-tert-Butylaniline may be used in the preparation of 2,3-bis(2-tert-butyl-phenyl-imino)butane. It may be used in the preparation of two rotamers, anti- and syn-N,N′-bis-(2-tert-butylphenyl)naphthalene-1,4,5,8-tetracarboxylic diimides and their guest inclusion abilities were investigated. | [General Description]
2-tert-Butylaniline is a sterically hindered aniline. 2-tert-Butylaniline participates in chemo- and regioselective copper-catalyzed cross-coupling reaction for the effective amination of 2-chlorobenzoic acids. |
|
|