444083-06-1

Usage

Properties

1. Molecular formula: C7H7NO3
2. Beta-amino aldehyde derivative
3. Propynyl substituent at the third position
4. Categorized as an azetidine
5. Four-membered ring containing nitrogen
6. 2R,3R stereochemistry
7. Presence of a methoxy and oxo group

Specific Content

1. Beta-amino aldehyde derivative with a propynyl substituent at the third position
2. Categorized as an azetidine, a saturated heterocyclic four-membered ring containing nitrogen
3. 2R,3R stereochemistry denotes the configuration of the chiral centers in the molecule
4. Contains a methoxy group and an oxo group
5. Potential applications in pharmaceuticals, agrochemicals, and material science, but further research is needed to understand its full range of uses and properties.

Upstream product

• 1031796-98-1 (3R,4S)-4-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-methoxy-1-prop-2-ynyl-azetidin-2-one 
• 214477-36-8 [1-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-meth-(E)-ylidene]-prop-2-ynyl-amine 

Downstream Products

• 1198184-51-8 C₁₈H₁₉NO₄ 

Relevant academic research and scientific papers

Structurally Novel Bi- and Tricyclic β-Lactams via [2 + 2] Cycloaddition or Radical Reactions in 2-Azetidinone-Tethered Enallenes and Allenynes

(Matrix presented) Thermolysis of β-lactam-tethered enallenyl alcohols gave tricyclic ring structures via a formal [2 + 2] cycloaddition of the alkene with the distal bond of the allene, while the tin-promoted radical cyclization in 2-azetidinone-tethered

Expeditious entry to enantiopure mono- and bis(tricyclic) β-lactams by single or double [2+2] cycloaddition of allenynes

A thermal methodology for the expeditious preparation of structurally novel strained tricyclic β-lactams containing a cyclobutene ring has been developed. Besides, the first examples accounting for the intramolecular double [2+2] cycloaddition of bis(alle