622-40-2 | 2-Morpholinoethanol

Packsize	Purity	Availability	Price	Discounted Price
100g	98%	in stock	$8.00	$6.00

Description

• Catalog Number: AI53850
• Chemical Name: 2-Morpholinoethanol
• CAS Number: 622-40-2
• Molecular Formula: C6H13NO2
• Molecular Weight: 131.17292
• MDL Number: MFCD00006180
• SMILES: OCCN1CCOCC1
• NSC Number: 1946

Computed Properties

• Complexity: 71.5
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: -0.8

Upstream Synthesis Route

2-Morpholinoethanol is a versatile compound extensively utilized in chemical synthesis as a crucial building block for the production of various chemicals and pharmaceuticals. Its key application lies in its role as a versatile amino alcohol, facilitating the synthesis of numerous complex molecules through its functional groups.One prominent application of 2-Morpholinoethanol is as a chiral ligand in asymmetric catalysis. This compound can form coordination complexes with transition metals, enabling enantioselective transformations in organic reactions. Its unique structural properties provide a stereochemical environment that promotes the selective formation of chiral products, essential in the synthesis of pharmaceutical intermediates and fine chemicals.Furthermore, 2-Morpholinoethanol serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its functionality allows for the introduction of amino and hydroxyl groups into target molecules, leading to the synthesis of diverse compounds with desired properties and biological activities.Overall, the versatility and reactivity of 2-Morpholinoethanol make it a valuable tool in chemical synthesis, enabling the construction of complex molecules and facilitating the development of new materials and pharmaceuticals.

Literature

• N-[4-(2-Morpholino-eth-oxy)phen-yl]acetamide monohydrate.

  Acta crystallographica. Section E, Structure reports online 20110201

• In vitro cytotoxicity of benzopyranone derivatives with basic side chain against human lung cell lines.

  Anticancer research 20101101

• Catalytic inhibition of topoisomerase II by a novel rationally designed ATP-competitive purine analogue.

  BMC chemical biology 20090101

• Noninfectious gastrointestinal (GI) complications of mycophenolic acid therapy: a consequence of local GI toxicity?

  Transplantation proceedings 20070101