472654
N-Boc-2-aminoacetaldehyde
95%
Synonyme(s) :
tert-Butyl N-(2-oxoethyl)carbamate
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About This Item
Produits recommandés
Niveau de qualité
Pureté
95%
Indice de réfraction
n20/D 1.455 (lit.)
Groupe fonctionnel
aldehyde
amine
Température de stockage
−20°C
Chaîne SMILES
CC(C)(C)OC(=O)NCC=O
InChI
1S/C7H13NO3/c1-7(2,3)11-6(10)8-4-5-9/h5H,4H2,1-3H3,(H,8,10)
Clé InChI
ACNRTYKOPZDRCO-UHFFFAOYSA-N
Informations sur le gène
human ... CTSK(1513)
Description générale
N-Boc-2-aminoacetaldehyde is an organic building block. It reacts with Horner-Wadsworth-Emmons (HWE) reagent to afford γ-aminobutyric acid (GABA)-derived α-keto amide/ester units.
Application
α-Methylenation of this amino aldehyde proceeds in a quick and efficient manner using a recently reported protocol involving formaldehyde and catalysis by either pyrrolidine proprionic acid or the dipeptide L-Pro-β-Ala.
Also used in a three-component synthesis of pyrrolidines involving 1,3-dipolar cycloaddition.
Also used in a three-component synthesis of pyrrolidines involving 1,3-dipolar cycloaddition.
N-Boc-2-aminoacetaldehyde may be employed in the following:
- As a starting reagent in the total synthesis of (+)-negamycin.
- Synthesis of (E)-ethyl 4-((tert-butoxycarbonyl)amino)but-2-enoate.
- Synthesis of 2,2′-bipyridine.
A building block in the synthesis of a protected pyrroloproline.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
235.4 °F - closed cup
Point d'éclair (°C)
113 °C - closed cup
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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