N-Benzylglycine ethyl ester, 97%
N-Benzylglycine ethyl ester, 97%
N-Benzylglycine ethyl ester, 97%
Thermo Scientific Chemicals

N-Benzylglycine ethyl ester, 97%

CAS: 6436-90-4 | C11H15NO2 | 193.25 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
500 g
Catalog number L15496.14
also known as L15496-14
Price (EUR)
50,60
Each
Quantity:
25 g
Request bulk or custom format
Price (EUR)
50,60
Each
Chemical Identifiers
CAS6436-90-4
IUPAC Nameethyl 2-(benzylamino)acetate
Molecular FormulaC11H15NO2
InChI KeyULOLIZHBYWAICY-UHFFFAOYSA-N
SMILESCCOC(=O)CNCC1=CC=CC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Refractive Index1.5030-1.5090 @ 20°C (non-U.S. specification)
Assay (GC)≥96.0%
Appearance (Color)Clear colorless to yellow
CommentSpecification differs for U.S. and non-U.S. material where indicated
N-Benzylglycine ethyl ester is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff field.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
N-Benzylglycine ethyl ester is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff field.

Solubility
Not miscible or difficult to mix in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Mu-Ill Lim.; Robert S. Klein.; Jack J. Fox. A new synthesis of pyrrolo[3,2-d]pyrimidines(9-deazapurines) via 3-amino-2-carboalkoxypyrroles. J. Org. Chem. 1979, 44 (22), 3826-3829.
  2. Tatsuya Shono.; Naoki Kise.; Takayoshi Tanabe. Electroorganic chemistry. 100. A new stereoselective method of synthesis of pyrrolizidines and indolizidines. J. Org. Chem. 1988, 53 (7), 1364-1367.