41365-75-7 | 1-Amino-3,3-diethoxypropane

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$23.00	$16.00
5g	97%	in stock	$45.00	$31.00
25g	97%	in stock	$137.00	$96.00
100g	97%	in stock	$435.00	$305.00

Description

• Catalog Number: AD29129
• Chemical Name: 1-Amino-3,3-diethoxypropane
• CAS Number: 41365-75-7
• Molecular Formula: C7H17NO2
• Molecular Weight: 147.2154
• MDL Number: MFCD00142581
• SMILES: NCCC(OCC)OCC

Computed Properties

• Complexity: 62.6
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 0.2

Upstream Synthesis Route

1-Amino-3,3-diethoxypropane, also known as ethyl 3-aminopropyl ether, is a versatile compound commonly utilized in various chemical synthesis applications. It serves as a valuable building block in organic chemistry due to its unique structure and reactivity.One prominent application of 1-Amino-3,3-diethoxypropane is its role as a nucleophilic amine species in the formation of C-N bonds. This compound can undergo nucleophilic substitution reactions with electrophiles, allowing for the introduction of the amino group into organic molecules. This capability makes it a key reagent in the synthesis of a wide range of nitrogen-containing compounds, including pharmaceuticals, agrochemicals, and organic materials.Furthermore, 1-Amino-3,3-diethoxypropane can also participate in various condensation reactions to form heterocyclic compounds. Its ability to react with carbonyl compounds, such as aldehydes and ketones, enables the formation of cyclic structures through the creation of imine intermediates. These heterocyclic compounds have diverse applications in medicinal chemistry, materials science, and the development of specialty chemicals.In addition to its involvement in the formation of C-N and C-C bonds, 1-Amino-3,3-diethoxypropane can serve as a protecting group for amines in organic synthesis. By temporarily masking the amino functionality with the ethoxypropyl moiety, chemists can selectively modify other reactive sites in a molecule without affecting the amine group. This strategy is particularly useful in multi-step syntheses where regioselectivity and functional group compatibility are crucial.Overall, the use of 1-Amino-3,3-diethoxypropane in chemical synthesis highlights its versatility and importance as a valuable reagent for constructing complex organic molecules with specific functionalities. Its ability to participate in diverse reactions and facilitate the efficient assembly of target compounds underscores its significance in modern synthetic chemistry.

Literature

• TiCl4-promoted cyclization reactions of aminoacetals and ethenetricarboxylates leading to nitrogen-containing heterocycles.

  The Journal of organic chemistry 20110805