1072-52-2 | 1-Aziridineethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$50.00	$35.00
5g	95%	in stock	$134.00	$94.00
10g	95%	in stock	$225.00	$158.00
25g	95%	in stock	$449.00	$315.00

Description

• Catalog Number: AB51394
• Chemical Name: 1-Aziridineethanol
• CAS Number: 1072-52-2
• Molecular Formula: C4H9NO
• Molecular Weight: 87.1204
• MDL Number: MFCD00005119
• SMILES: OCCN1CC1
• NSC Number: 50209

Computed Properties

• Complexity: 42.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: -0.6

Upstream Synthesis Route

1-Aziridineethanol, also known as aziridin-1-ylethanol, is a versatile compound widely used in chemical synthesis. This unique molecule contains both an aziridine ring and a hydroxyl functional group, making it a valuable building block in organic chemistry.In chemical synthesis, 1-Aziridineethanol serves as a key intermediate in the preparation of various important compounds. Its aziridine ring can undergo ring-opening reactions to form diverse products with different functional groups. This property makes 1-Aziridineethanol a valuable precursor for the synthesis of a wide range of pharmaceuticals, agrochemicals, and specialty chemicals.Furthermore, the hydroxyl group in 1-Aziridineethanol allows for easy derivatization, enabling the introduction of additional functionalities or modifications to the molecule. This flexibility makes 1-Aziridineethanol a versatile starting material for the development of new chemical entities with desired properties.Overall, the application of 1-Aziridineethanol in chemical synthesis is essential for the construction of complex molecules and the discovery of novel compounds with potential uses in various industries.

Literature

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  International journal of nanomedicine 20100101

• Regioselective synthesis of N-beta-hydroxyethylaziridines by the ring-opening reaction of epoxides with aziridine generated in situ.

  Organic letters 20060316

• New insights into the reaction of zinc alkyls with dioxygen.

  Journal of the American Chemical Society 20031022

• Formation of two diverse classes of poly(amino-alkoxide) chelates and their mononuclear and polynuclear lanthanide(III) complexes.

  Inorganic chemistry 20030811

• Fragmentation of dipyridamole and related dipyrimidines by electrospray ionization collisional activated decomposition mass spectrometry.

  Journal of mass spectrometry : JMS 20030501

• Copolymers of ethylene imine and N-(2-hydroxyethyl)-ethylene imine as tools to study effects of polymer structure on physicochemical and biological properties of DNA complexes.

  Bioconjugate chemistry 20020101