136964

Sigma-Aldrich

N-Isopropylbenzylamine

97%

Synonym(s):
N-Benzylisopropylamine
Linear Formula:
C6H5CH2NHCH(CH3)2
CAS Number:
Molecular Weight:
149.23
Beilstein/REAXYS Number:
2638437
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

assay

97%

refractive index

n20/D 1.502 (lit.)

bp

200 °C (lit.)

density

0.892 g/mL at 25 °C (lit.)

SMILES string

CC(C)NCc1ccccc1

InChI

1S/C10H15N/c1-9(2)11-8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

InChI key

LYBKPDDZTNUNNM-UHFFFAOYSA-N

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General description

N-Isopropylbenzylamine forms amine adducts with magnesocene at ambient temperature in toluene.

Application

N-Isopropylbenzylamine was used as ligand in the preparation and characterization of bis(cyclopentadienyl)magnesium. It was also used in the synthesis of N-benzylideneisopropylamine-N-oxide.

Packaging

25 g in glass bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Hazard Codes

Xi

Risk Statement

36/37/38

Safety Statement

26-36

WGK Germany

WGK 3

Flash Point(F)

161.6 °F - closed cup

Flash Point(C)

72 °C - closed cup

Aibing Xia et al.
Journal of the American Chemical Society, 124(38), 11264-11265 (2002-09-19)
Magnesocene adducts of alkylamines were prepared and characterized. Treatment of 3-amino-2,4-dimethylpentane, isopropylamine, tert-butylamine, benzylamine, or N-isopropylbenzylamine with magnesocene at ambient temperature in toluene afforded the amine adducts Cp2Mg(NH2CH(CH(CH3)2)2) (91%), Cp2Mg(NH2iPr) (80%), Cp2Mg(NH2tBu) (67%), Cp2Mg(NH2CH2Ph) (80%), and Cp2Mg(NH(CH(CH3)2)(CH2C6H5)) (91%). These adducts...
One-flask transformation of secondary amines to nitrones by oxidation with hydrogen peroxide mediated by triscetylpyridinium tetrakis oxodiperoxotungsto-phosphate (PCWP). Some mechanistic considerations.
Ballistreri FP, et al.
Tetrahedron, 48(40), 8677-8684 (1992)
O Brüggemann
Biomolecular engineering, 18(1), 1-7 (2001-06-29)
Molecular imprinting is a way of creating polymers bearing artificial receptors. It allows the fabrication of highly selective plastics by polymerizing monomers in the presence of a template. This technique primarily had been developed for the generation of biomimetic materials...

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