645-36-3 | Aminoacetaldehyde diethyl acetal

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$9.00	$6.00
50g	98%	in stock	$15.00	$10.00
100g	98%	in stock	$25.00	$17.00

Description

• Catalog Number: AB43542
• Chemical Name: Aminoacetaldehyde diethyl acetal
• CAS Number: 645-36-3
• Molecular Formula: C6H15NO2
• Molecular Weight: 133.1888
• MDL Number: MFCD00008136
• SMILES: NCC(OCC)OCC
• NSC Number: 19501

Computed Properties

• Complexity: 53
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 5
• XLogP3: -0.1

Upstream Synthesis Route

2,2-Diethoxyethanamine, also known as diethoxyethylamine, is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as an important building block in organic chemistry, particularly in the development of various pharmaceuticals, agrochemicals, and materials.One of the key applications of 2,2-Diethoxyethanamine is in the formation of amine-based ligands and catalysts. By utilizing its amine functional group, this compound can participate in various reactions such as reductive amination, where it acts as a nucleophile to form stable carbon-nitrogen bonds. These amine-based ligands and catalysts then play crucial roles in facilitating a wide range of organic transformations with high efficiency and selectivity.Furthermore, 2,2-Diethoxyethanamine can be utilized as a protecting group in organic synthesis. Its diethoxyethyl group can temporarily shield sensitive functional groups or reactive sites in complex molecules, allowing selective reactions to take place without unwanted side reactions. This protective strategy enables chemists to manipulate and modify molecules in a controlled manner, leading to the synthesis of intricate chemical structures with precision.In summary, the application of 2,2-Diethoxyethanamine in chemical synthesis is diverse and significant. From serving as a key building block for amine-based ligands and catalysts to acting as a protective group in complex molecule synthesis, this compound plays a crucial role in advancing the field of organic chemistry.

Literature

• Concise stereocontrolled formal synthesis of (+/-)-quinine and total synthesis of (+/-)-7- hydroxyquinine via merged Morita-Baylis-Hillman-Tsuji-Trost cyclization.

  The Journal of organic chemistry 20081205

• A derivative of diethylenetriaminepentaacetic acid for europium labeling of proteins.

  Bioconjugate chemistry 20010101