Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C6H5CH2NHCH2CH2NH2
CAS Number:
Molecular Weight:
150.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-984-5
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.54 (lit.)
bp
162 °C/20 mmHg (lit.)
density
1 g/mL at 25 °C (lit.)
functional group
amine, phenyl
SMILES string
NCCNCc1ccccc1
InChI
1S/C9H14N2/c10-6-7-11-8-9-4-2-1-3-5-9/h1-5,11H,6-8,10H2
InChI key
ACYBVNYNIZTUIL-UHFFFAOYSA-N
General description
N-Benzylethylenediamine participates in the one-pot synthesis of N,N,N′-trisubstituted guanidines. It undergoes condensation with dibenzoylmethane (1,3-diphenyl-1,3-propanedione) in stoichiometric ratio 1:1 to afford the corresponding Schiff monobase.
Application
N-Benzylethylenediamine may be used for the synthesis of N-benzyl-N,N′,N′-tris(tert-butyloxycarbonylmethyl)ethylenediamine and 3-benzyl-2-(phenyl-2-sulfonate)-2-imidazoline tetraheptylammonium salt.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
203.0 °F - closed cup
flash_point_c
95 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Nickel (II) Complexes of Dibenzoylmethane and N-benzylethylenediamine, and Their Schiff Monobase.
Gutierrez JA, et al.
Journal of Coordination Chemistry, 28(3-4), 305-312 (1993)
A new method for the synthesis of tri-tert-butyl diethylenetriaminepentaacetic acid and its derivatives.
Achilefu S, et al.
The Journal of Organic Chemistry, 65(5), 1562-1565 (2000)
Anthony Weatherwax et al.
Organic letters, 7(16), 3461-3463 (2005-07-29)
Trans-disubstituted beta-lactams show increasing utility and prominence in numerous pharmaceutical applications, making their asymmetric synthesis an attractive goal for chemists. We introduce an anionic, nucleophilic catalyst system that provides an efficient, diastereoselective route to trans-disubstituted beta-lactams, a complement to our
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 462292-25ML | 04061832346397 |
| 462292-5ML | 04061836820572 |
