6723-30-4 | O-(Tetrahydro-2H-pyran-2-yl)hydroxylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$9.00	$7.00
5g	97%	in stock	$17.00	$12.00
10g	97%	in stock	$24.00	$17.00
25g	97%	in stock	$51.00	$36.00
100g	97%	in stock	$183.00	$128.00

Description

• Catalog Number: AB46814
• Chemical Name: O-(Tetrahydro-2H-pyran-2-yl)hydroxylamine
• CAS Number: 6723-30-4
• Molecular Formula: C5H11NO2
• Molecular Weight: 117.1463
• MDL Number: MFCD01321374
• SMILES: NOC1CCCCO1

Computed Properties

• Complexity: 67.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.2

Upstream Synthesis Route

O-Tetrahydroxy-Pyran-2-yl-Hydroxylamine, commonly referred to as $name$, plays a crucial role in chemical synthesis as it serves as a versatile reagent with various applications. In organic chemistry, $name$ is commonly utilized as a powerful reducing agent due to its ability to donate electrons and facilitate reduction reactions. This compound is particularly valuable in the reduction of carbonyl compounds, such as aldehydes and ketones, to produce corresponding alcohols.Furthermore, $name$ can also be employed in the synthesis of various heterocyclic compounds. Its unique structure allows for the formation of cyclic structures, enhancing its usefulness in the creation of complex organic molecules. Additionally, $name$ has found utility in the preparation of pharmaceutical intermediates, enabling the efficient synthesis of biologically active compounds.Overall, the versatility of O-Tetrahydroxy-Pyran-2-yl-Hydroxylamine in chemical synthesis makes it a valuable tool for organic chemists seeking to efficiently carry out a wide range of reactions and syntheses.

Literature

• Accumulation of true single strand breaks and AP sites in base excision repair deficient cells.

  Mutation research 20101210