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Glycine tert-butyl ester, 97%, Thermo Scientific Chemicals
Catalog number: L16258.06
5 g, Each
Thermo Scientific Chemicals
Glycine tert-butyl ester, 97%, Thermo Scientific Chemicals
Catalog number: L16258.06
5 g, Each
Quantity
Catalog number: L16258.06
also known as L16258-06
Price (USD)
Price: 271.00
Online price: 236.65
Your price:
Quantity
-
Chemical Identifiers
CAS
6456-74-2
IUPAC Name
tert-butyl 2-aminoacetate
Molecular Formula
C6H13NO2
InChI Key
SJMDMGHPMLKLHQ-UHFFFAOYSA-N
SMILES
CC(C)(C)OC(=O)CN
Specifications
Specification SheetAppearance (Color)
Clear colorless to yellow
Assay (GC)
≥95.0%
Form
Liquid
Refractive Index
1.4215-1.4265 @ 20°C
Description
Glycine tert-butyl ester is used in the preparation of Schiff base by reacting with benzophenone. The resultant Schiff base undergoes asymmetric alkylation with arylmethyl bromides in the presence of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide as chiral phase transfer catalyst to give guanidine-containing pentacyclic compound.
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
Glycine tert-butyl ester is used in the preparation of Schiff base by reacting with benzophenone. The resultant Schiff base undergoes asymmetric alkylation with arylmethyl bromides in the presence of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide as chiral phase transfer catalyst to give guanidine-containing pentacyclic compound.
Solubility
Miscible with acetone and methanol. Slightly miscible with ehtanol. Immiscible with water.
Notes
Air sensitive. Store in a cool place. Incompatible with strong oxidizing agents.
Glycine tert-butyl ester is used in the preparation of Schiff base by reacting with benzophenone. The resultant Schiff base undergoes asymmetric alkylation with arylmethyl bromides in the presence of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide as chiral phase transfer catalyst to give guanidine-containing pentacyclic compound.
Solubility
Miscible with acetone and methanol. Slightly miscible with ehtanol. Immiscible with water.
Notes
Air sensitive. Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only
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