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469637

Sigma-Aldrich

N-Benzylidene-tert-butylamine

98%

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Linear Formula:
C6H5CH=NC(CH3)3
CAS Number:
6852-58-0
Molecular Weight:
161.24
MDL number:
MFCD00043553
UNSPSC Code:
12352100
PubChem Substance ID:
24870474
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.52 (lit.)

bp

209 °C (lit.)

density

0.906 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)\N=C\c1ccccc1

InChI

1S/C11H15N/c1-11(2,3)12-9-10-7-5-4-6-8-10/h4-9H,1-3H3/b12-9+

InChI key

KFLSWDVYGSSZRX-FMIVXFBMSA-N

General description

In vitro metabolism of N-benzyl-tert-butylamine in male hamster hepatic microsomal preparations has been studied. Kinetic studies of frustrated Lewis pair (FLP)-catalyzed hydrogenation and deuteration of N-benzylidene-tert-butylamine suggests that the reaction proceeds via autoinductive catalysis.

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Sebastian Tussing et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(22), 8056-8059 (2015-04-17)
The frustrated Lewis pair (FLP)-catalyzed hydrogenation and deuteration of N-benzylidene-tert-butylamine (2) was kinetically investigated by using the three boranes B(C6F5)3 (1), B(2,4,6-F3-C6H2)3 (4), and B(2,6-F2-C6H3)3 (5) and the free activation energies for the H2 activation by FLP were determined. Reactions
M Ulgen et al.
Drug metabolism and drug interactions, 12(2), 131-143 (1995-01-01)
The metabolism of N-benzyl-tert-butylamine was studied in vitro using male hamster hepatic microsomal preparations. This substrate produced the corresponding nitrone, benzaldehyde and an uncharacterised metabolite. No metabolites were detected which corresponded to either authentic amide or oxaziridine. The results indicate

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