CAS 6456-74-2
:Glycine tert-butyl ester
Description:
Glycine tert-butyl ester, with the CAS number 6456-74-2, is an organic compound that serves as an amino acid derivative. It features a glycine backbone, where the amino group is protected by a tert-butyl ester group. This structure imparts several notable characteristics. Glycine tert-butyl ester is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water due to the hydrophobic tert-butyl group. The compound is often used in peptide synthesis and as an intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the ester functional group, which can undergo hydrolysis or transesterification under appropriate conditions. Additionally, glycine tert-butyl ester is generally considered to have low toxicity, making it a useful reagent in laboratory settings.
Formula:C6H13NO2
InChI:InChI=1/C6H13NO2/c1-6(2,3)9-5(8)4-7/h4,7H2,1-3H3
SMILES:CC(C)(C)OC(=O)CN
Synonyms:- tert-Butyl glycinate
- H-Gly-OtBu
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
Glycine tert-butyl ester, 97%
CAS:<p>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 gua</p>Formula:C6H13NO2Purity:97%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:131.18DL-Glycine tert-butyl ester
CAS:<p>DL-Glycine tert-butyl ester</p>Formula:C6H13NO2Purity:97%Color and Shape: clear. colourless liquidMolecular weight:131.17g/moltert-Butyl glycinate
CAS:<p>tert-Butyl glycinate is a synthetic reagent that contains a tert-butyl group. It is used in analytical chemistry to determine the concentrations of cinchonidine and ester hydrochloride in the reaction solution. This can be done by adding trifluoroacetic acid to the reaction solution, which causes the formation of tert-butyl glycinate. The hydrogen chloride from this reaction will react with sodium carbonate, forming hydrogen gas and sodium bicarbonate. The presence of nitrogen atoms on the tert-butyl glycinate molecule allows for an asymmetric synthesis, which can be used to synthesize serine protease.</p>Formula:C6H13NO2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:131.17 g/moltert-Butyl 2-aminoacetate
CAS:Formula:C6H13NO2Purity:95.0%Color and Shape:Brown liquidMolecular weight:131.175




