31576-51-9 | 2-(2-Methoxyethoxy)ethanamine

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$13.00	$9.00
1g	98%	in stock	$33.00	$23.00
5g	98%	in stock	$65.00	$45.00
10g	98%	in stock	$110.00	$77.00
25g	98%	in stock	$232.00	$162.00

Description

• Catalog Number: AB51205
• Chemical Name: 2-(2-Methoxyethoxy)ethanamine
• CAS Number: 31576-51-9
• Molecular Formula: C5H13NO2
• Molecular Weight: 119.1622
• MDL Number: MFCD09261088
• SMILES: COCCOCCN

Computed Properties

• Complexity: 41.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 5
• XLogP3: -1.2

Upstream Synthesis Route

2-(2-Methoxyethoxy)ethanamine is a versatile compound that finds significant application in chemical synthesis processes, particularly in organic and medicinal chemistry. This compound serves as a crucial building block for the synthesis of various pharmaceutical drugs, agrochemicals, and organic materials due to its unique chemical structure and reactivity.In chemical synthesis, 2-(2-Methoxyethoxy)ethanamine acts as a valuable intermediate in the production of specialized organic molecules. Its functional groups enable it to participate in a wide range of reactions, including nucleophilic substitutions, condensations, and cyclizations, leading to the formation of complex molecular structures. This compound is often utilized in the preparation of advanced intermediates that are further transformed into final products with desired properties.Additionally, the presence of the methoxyethoxy group in 2-(2-Methoxyethoxy)ethanamine imparts specific characteristics to the molecules it is incorporated into. These properties can influence the bioavailability, stability, and potency of the final products, making this compound crucial for the fine-tuning of chemical structures in drug discovery and development.Overall, 2-(2-Methoxyethoxy)ethanamine plays a pivotal role in chemical synthesis by enabling the efficient construction of diverse organic compounds with tailored functionalities and applications. Its versatility and reactivity make it an indispensable tool for researchers and chemists working in the fields of drug design, material science, and biotechnology.

Literature

• Substrate properties of C5-substituted pyrimidine 2'-deoxynucleoside 5'-triphosphates for thermostable DNA polymerases during PCR.

  Bioorganic & medicinal chemistry letters 20031103

• Simultaneous incorporation of three different modified nucleotides during PCR.

  Nucleic acids research. Supplement (2001) 20030101