Glycine tert-butyl ester, 97%
Glycine tert-butyl ester, 97%
Glycine tert-butyl ester, 97%
Glycine tert-butyl ester, 97%
Thermo Scientific Chemicals

Glycine tert-butyl ester, 97%

CAS: 6456-74-2 | C6H13NO2 | 131.175 g/mol
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Catalog NumberQuantity
ALFL16258.065 g
Catalog number ALFL16258.06
Price (MYR)
1,440.00
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5 g
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Price (MYR)
1,440.00
EA
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Specifications
Chemical Name or MaterialGlycine tert-butyl ester
CAS6456-74-2
Boiling Point29°C to 31°C (2mmHg)
Recommended StorageKeep cold; Store under Argon
TSCANo
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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.
RUO – Research Use Only

General References:

  1. Lou, S.; Ramirez, A.; Conlon, D. A. Catalytic syn-Selective Direct Aldol Reactions of Benzophenone Glycine Imine with Aromatic, Heteroaromatic and Aliphatic Aldehydes. Adv. Synth. Catal. 2015, 357 (1), 28-34.
  2. Peng, Z.; McLuckey, S. A. C-terminal peptide extension via gas-phase ion/ion reactions. Int. J. Mass Spectrom. 2015, 391, 17-23.